A.H.A Group is a leading global provider of ingredients solution, specializes in Pharmaceuticals, Nutraceuticals, Food& Beverage industries more than 25 years, with approximately 200 employees worldwide, annual turnover of USD200 millions. The main products cover Amino Acids, Vitamins, Herb Extracts and Nutritional Supplements.
Accuprec Research Labs
Pvt. Ltd. ® is the FDCA approved, NABL, ISO 9001:2015, GLP,
CPCSEA & ISO/IEC 17025 accredited Contract Research Organisation
(CRO) having head quarter at Ahmedabad, Gujarat and having branch office at Sudbury,
Canada and Pensylvenia, USA. Accuprec® is a service provider for
various testing services required for pharmaceuticals, chemicals,
phytochemicals, herbal formulations, food and Medical devices. Accuprec has
been founded by a group of highly qualified professionals having excellent
track record with proven success and commitment to quality in their respective
areas of expertise.
At Accuprec, we offers below mentioned various services in 14 verticles:
· Analytical (HPLC/UV) method development & Validation (AMV) & Regulatory testings
· Bio-compatibility testings for Medical devices (As per ISO 10993 guidelines)
· Cell-line based testings (In-vitro toxicity & efficacy studies)
· Chemical & Pigment testing (For Textile and Pigment industry)
· Clinical services (BA/BE, PMS) (As per ICMR / ICH-GCP guideline)
· Formulation & Development Services (Upto Pilot scale & Tech Transfer)
· Food Testing (As per FSSAI guidelines)
· IPR management services (Patent, TM, Design and Copyright drafting, filing, Valuation of IP)
· Microbiological & Sterility testing (As per IP/BP/ USP & Method development also)
· Phytochemical studies (Heavy metal testings using ICP-OES)
· Pharmacological screening (In-vitro / In-vivo)
· Stability studies (As per ICH guidelines)
· Regulatory Dossier preparation for regulated and non-regulated market (CTD & e-CTD format)
· Toxicological testing (in-vitro, ex-vivo and in-vivo) (As per OECD / Schedule Y /AYUSH guidelines)
Top of Form Akums Drugs & Pharmaceuticals Limited, India is an emerging global pharma manufacturing company. Six State-of-the-art manufacturing facilities producing Tablets, Capsules (Hard/Soft) Liquid Orals, Dry Syrups, Injectables (Dry/Liquid), SVP's, LVP's, Eye/Ear Drops, Pre-Filled Syringes, Sachets, Effervescent & Mouth Dissolving Tablets, Ointments, Hormones, Nutraceuticals, Cosmetics etc. We have largest manufacturing capacities and are associated with leading Indian as well as MNC's. We specialize in offering the following:
Novel Drug Delivery System based innovative formulations
Research & Development of New Formulations
Technology Development and Transfer
We seek alliances / JV's for International markets.
Altova Healthcare group has its manufacturing setup Blossom Pharmaceuticals at Goa, manufacturing: Non-Sterile Creams, Ointments, Lotions, Gels, Ear drops, Solutions and provides Product Development Services since 1995. Backed by extensive manufacturing, marketing experience & widespread distribution network, Altova Healthcare is one of the most innovative and dynamic companies in India. The facility is WHO-GMP(India) certified and complies with US-FDA, NAFDAC and ISO 9001:2015. Our facility is registered with Srilanka and Ivory-Coast MOH.
Anton Paar develops and produces high-quality measuring and analysis instruments for industrial and research applications. Founded in 1922, Anton Paar is the world leader in density, concentration and CO2 measurement and in the field of rheometry. The state-of-the-art product range also comprises small-angle X-ray scattering systems, instruments for surface characterization, viscometers, refractometers, polarimeters, microwave synthesizers, microwave digesters, petroleum testing instrumentation and a range of process instruments.
Anton Paar India Pvt. Ltd. is headquartered at Gurgaon - NCR Delhi. The sales and service centers are located in Mumbai, Kolkata, Chennai, Bangalore, Hyderabad, Vadodara, Ahmedabad and Guwahati and there are four application support centers in Gurgaon, Mumbai, Bangalore and Hyderabad.
Aurisco is an innovative company dedicated to developing and manufacturing pharmaceutical chemicals serving pharmaceutical companies worldwide. With 2 manufacturing sites for chemistry synthesis & fermentation, all of which are operated according to cGMP standards, Aurisco offers Active Pharmaceutical ingredients (APIs especially in segments of Steroids, Oncology, Anti-Virus and etc.) and drug intermediates as well as contract developing and manufacturing of pharmaceutical chemicals from kilos to tons.
AUTOCAL SOLUTIONS PVT. LTD. is a pan India Company with a local focus. Established in 2002, we have capability to offer our customers localized support and service when and where required. By continuing to expand our laboratory network, we provide support for the growing needs of our customers both locally & internationally. Our Principle Laboratory in Vasai is accredited by NABL as per the requirements of ISO/IEC 17025:2005.
Our areas of expertise include Calibration, Thermal Validation and Clean Room Validation.
As an Industry leader, Autocal with a team of 150 plus well experienced and Qualified Engineers/Technicians offers services at our laboratory as well as onsite and has till date provided services to more than 1300 multinational and national companies through its wide spread network of 9 branches in Aurangabad, Bhandup (Mumbai), Baddi, Panaji (Goa), Indore, Vapi, Hyderabad. These Labs are equipped with the latest range of equipments and are constantly being upgraded to meet the changes in technology and customer needs.
Autocal's procedures are in accordance with National/International Standards like EN 554, EU & ISO/IEC 17025. All validations are 21 CFR part 11 compliant and we feel proud that during client audits our work has been well appreciated by several international agencies including USFDA, MHRA, MCC, TGA, WHO (Geneva), ISO, TS and other CRAM audits.
Beijing Huikang Boyuan Chemical Tech Co Ltd established in 2005 is a high-tech enterprise and specializes in research and manufacture of new drugs, APIs and pharmaceutical intermediates.
Beijing Infoark Co Ltd, established in 1997, specializes in pharmaceuticals, intermediates, food and feed additives, veterinary, health and nutrition products. After years of rapid development, Infoark has become one of the largest and most professional suppliers in China, and grows to be an integrated company covering R&D, production and sales, with international trade as the main development direction based upon the leading high-tech R&D and production site.
Brooks Laboratories Ltd was established in 2002 and maintains its strong presence in the Pharmaceutical industry as a Contract Manufacturing Company since its inception. Brooks Laboratories Ltd is a Research and Development driven Pharmaceutical manufacturing company. In last 6 years company has successfully established itself as a reputed Contract Manufacturing company for generic products in Injectables and Amoxiillin + Clavulanic Acid range of Tablets and Dry Syrups. Brooks has recently commissioned a Brand New Dedicated Facility for Carbapenem Injections at Baroda, India, with a huge capacity of 50 million vials per annum. The New Carbapenem Facility at Baroda will also manufacture Lyophilized Carbapenem injections like Ertapenem. The new Dedicated Carbapenem Plant has been designed for Development and Supply of Injections for Europe, USA, Canada, Australia, South Africa and other Regulated Markets and also do Contract Manufacturing for Quality Conscious Pharmaceutical companies for Regulated and Semi Regulated Markets. Brooks can as well provide interested customers with ANDAs and Dossiers in CTD formats. The new Plant at Baroda has good capacity to cater to big markets of USA, Europe etc. The entire new plant of Carbapenems at Baroda has been designed as per the cGMP requirements of US-FDA, European GMP standards and WHO standards. The Carbapenem plant is scheduled for a European GMP audit and certification in August '2017. Interested parties for Carbapenems and other injections can contact us - [email protected]
Established in 1996, Capot Chemical Co Ltd is a custom synthesis manufacturer, headquartered in Hangzhou, P.R.China. As an ISO 9001:2008 certificated company, Capot has a safety management system in place. It produces a wide range of organics, especially fluorine, boronic acids, unnatural amino acids, cross linkers, chiral building blocks, heterocyclic compounds and other active pharmaceutical ingredients. Capot has established a global network of customers from many research centers, pharmaceutical companies and chemical factories.
Capot has experienced experts, excellent manufacturing equipment, and a advanced R&D center. It owns the ability to provide products from a few grams to kilograms, even to tons. And it also provides custom synthesis service, to help its customer with its best efforts.
In capot, we care about the quality and success of our customers' projects as if they were our own. We are committed into providing the reliable quality, competitive prices and superior service to our customers.
- Pharmaceutical Technology, Laboratory and Analytical Equipment
- Custom Manufacturing/Exclusive Synthesis of Fine Chemicals
- Contract Services - Contract Services
- Intermediates, Fine and Specialty Chemicals
- Advanced Intermediates
- Contract Manufacturing
- Pharmaceutical Technology (general category)
- Custom Manufacturing
CCPIT Sub-council of Chemical Industry and CCOIC Chemical Industry Chamber of Commerce are the branch organizations of CCPIT and CCOIC. They belong to China Petroleum and Chemical Industry Federation (CPCIF) and work as the CPCIF Conference and Exhibition Department. CCPIT Sub-council of Chemical Industry is a certified member of UFI and Shanghai Convention & Exhibition Industries Association (SCEIA).
We aim to promote trade, economic and technological cooperation between foreign countries and China. Based on serving the entire chemical industry and our member companies, we will make the best efforts to promote the development of chemical industry.
Organizing exhibitions and conferences is our main channel of promoting domestic and overseas economic and trade exchange, however, we organize domestic enterprises to go abroad, hosting and participating in professional chemical industry exhibitions.
Chemical Information Services has collected and distributed vital information for the chemical and pharmaceutical industry for over 40 years. Our paid subscribers have more than $750 billion in purchasing power annually representing close to 50% of the world's chemical purchasing professionals. In 2014 we rebranded our modules and launched the NextGeneration of our database that integrated our four products: Directory of World Chemical Producers (DWCP), FinishedForms, PathFinder, and ContractManufacturing. This integration allows our users to have access to more comprehensive data and a better user experience. Each of the modules is geared to help buyers and sellers in the chemical industry with their procurement, sourcing, sales and marketing initiatives. We continually update our databases with the help of our in-house Research Department of chemists and through direct contact with companies, relationships with trade associations and our network of global affiliates.
Biopurify is a leading company in R&D, manufacture and marketing of High Quality Phytochemicals and Extracts (especially Active Ingredients from Chinese Herbs), Natural Active Pharmaceutical Ingredients worldwide. From small quantities for R&D or reference standard to large quantities for customizing or manufacturing, Biopurify emphasizes the service featuring consistency and reliability.
This site is in-compliance with USFDA, MHRA, ICH, TGA, MCC & PIC/S regulatory requirements.
We are looking for the contract manufacturing (site transfer / technology transfer ) , development & out-licensing opportunities for EUROPE, US, Canada, Australia,, South Africa and PIC/S markets.
We are the biggest professional company with years of experience in technology transfer and commercialization in China. With our broad, global network and extensive recourses, we devote ourselves to delivering professional services, including technology transfer, patent licensing, consulting, co-investment & technology incubation as well as public service.
We are entrusted by Tsinghua University,one of the top universities in China, to commercialize Tsinghua University's scientific and technological achievements, to carry out technology commercialization and technology management of International Technology Transfer Center (ITTC) of Tsinghua University.
Pharma Reference Standards, Research Chemicals, & Services like Contract Research & Manufacturing Services. (CRO & CRAMS)
Tyvek® medical and pharmaceutical packaging provides durability, compatibility with a wide range of sterilization methods, and the highest microbial barrier of any breathable sterile packaging material.
DuPont™ Tyvek™ Air Cargo Covers are used to protect a wide variety of healthcare products worldwide to prevent temperature excursions during transportation.
DuPont™ Tyvek® IsoClean® delivers an ideal balance of protection, durability and comfort. Garments made of Tyvek® IsoClean® are used in the biotech, pharmaceutical, medical device manufacturing as well as in other critical or controlled environments ensuring superior protection for your business critical systems, equipment and controlled environment production processes.
It's a truly dynamic time for the global pharma industry, and CPhI Worldwide & P-MEC India provides an opportunity to meet the GEA team, discover the latest trends, technologies and insights and, above all else, drive new partnerships, do business and grow. By investing in and supporting these events, we're highlighting our ongoing support for the current and future pharmaceutical industry. Learn all about GEA's solutions for the Solid-Pharma, Liquid-Pharma and Bio-Pharma industries. Get ‘hands on' with our equipment for batch and continuous productions and take part in "live" demonstrations and meet all our experts from every sector of the pharmaceutical market in one place.
The Glatt Group has been involved in powder technology for over 50 years and has become renowned as one of the world's major manufacturers in fluid beds for the pharmaceutical industries, specialising in techniques for solid product forms for the food, feed, pharmaceutical and fine chemical industries.Besides pilot and production equipment for both batch and continuous processing Glatt has further extended to a wide range of processing lines, offering product and process development, contract manufacturing, plant design and engineering services.
At GMP Compliance LTD we are a team of highly skilled and passionate individuals who together offer a valuable support and consultancy service to the pharmaceutical and food supplement industry in regards to Good Manufacturing Practice. We truly love what we do. We get it right in an industry where getting it wrong is not an option. Our clients feel secure in the knowledge that we have the right experience, qualifications and drive to deliver the right results. GMP Compliance LTD offer support and guidance by providing the following services:Validation Services:
- Computer Systems, Documentation Systems, Equipment, URS/IQ/OQ/PQ generation, Project Management, Method.
- IRCA Certified Lead Auditors, API, QP, CMO, Packaging, Pre Inspection, Gap Analysis, Cosmetic, Medical Device, ISO, Computer Systems, GMDP, GCP, PV.
- Documentation Support, QA Support, Contract QP/RP, Production Advice, Self Inspections.
- Technical Transfer, Project Management, Supplier Sourcing, Regulatory Support, Licensing Support, Excipient Risk Assessment.
- Monthly open training days, GMP, PQS, Technical Transfer, GDP.
groninger, the name stands for innovation, quality and service in the design of customized machines for the Pharmaceutical, Cosmetics and Consumer Healthcare industry. We have proven it to our customers for 37 years.
Customer focus for groninger is more than simply meeting the requirements of our customers. It is our goal to meet the challenges of the future through research and development and to offer innovative solutions. 1100 employees, in Crailsheim, Schnelldorf and Charlotte (North Carolina, USA), work to provide solutions and to optimize processes – fulfilling our company philosophy "We fill Visions with Life"?.
This is how groninger has become a technology leader in building customized machines for the Pharmaceutical, Cosmetics and Consumer Healthcare industry. To remain successful in this field, we must not only know our customers and their industries but we must also understand them. Trust in our own skills, working cooperatively together within our company and with customers form the basis for bringing visions to life, creating unique solutions and making our customers enthusiastic.
Our experience since more than 37 years, guarantees safe production processes and excellent results for our customers. The competence and enthusiasm of our employees are the basis of the extremely successful development of our company.
- Products: Custom-built machines for the pharmaceutical, cosmetic and consumer healthcare industry
- Sites: Crailsheim, Schnelldorf, Charlotte (USA)
- Agencies: Worldwide in more than 35 countries
- Established: 1980 by Eva and Horst Groninger
- Management: Jens Groninger in Crailsheim, Volker Groninger in Schnelldorf, Horst and Eva Groninger in the holding board
- Employees: Worldwide 1,135 (as of April 2017)
- Revenue: 156 million euros (in 2016)
Headquartered in Hyderabad, India, GVK Biosciences is one of Asia's leading Discovery Research and Development organizations. GVK BIO provides a broad spectrum of services, across the Research and Development and manufacturing value chain with a focus on speed and quality. GVK BIO capabilities include Integrated Programs, Discovery Services, Clinical Development, Contract Manufacturing, Formulations and Informatics. GVK BIO's 2400 employees serve a diverse and global customer base of more than 350 satisfied customers.
We are manufacturer of three dimensional blender / mixer. 3D mixing is the latest technology for uniform / homogeneous mixing of powder and/or liquids. The motion is based on kinematic inversion principle, which gives faster mixing. It is 4 to 5 times more faster to give uniform mixing than conventional mixers.
Hexagon has state of the art manufacturing and R & D facility at our plant in Vadodara. We offer this mixer in laboratory, pilot and production capacity. Our mixer models of 3 ltr, 10 ltr, 20 ltr, 35 ltr, 50 ltr and 75 ltr are offered as standard models. Models 90 ltr and above are customized to suit customer drum dimensions. We offer mixer up to 500 ltr and even larger.
THE HOSOKAWA MICRON GROUP
The Companies of the Hosokawa Micron Group offer a comprehensive range of services on the sector of technology, machine design and system engineering in accordance with all national and international pharmaceutical quality standards and have become a market and technological leader when it comes to mixing, blending, drying, grinding, micronising, jet milling, classifying, compacting, agglomerating, filling and weighing of powders and particles used to make tablets, capsules, granules, infusions and injection solutions as well as high-tech solutions for sterile processing systems.
HOSOKAWA ALPINE Aktiengesellschaft, Augsburg, Germany
Formed in 1898, Hosokawa Alpine's range includes the development, design and manufacture of components and turnkey systems to produce powders, granules and bulk materials for the chemical, pharmaceutical, food, minerals, metals and recycling industries.
The name ALPINE stands for competence in all areas of comminution technology. The long years of close cooperation between our engineers and the development departments of our customers have made us leading specialists for powder and particle processing technology around the world. Because our aim is to offer our customers the very best in professional and accomplished advice tailored to their specific branch of industry, our powder and particle processing division is divided into the subdivisions Pharma & Food, Chemicals, Minerals & Metals, Recycling & Granulators and Service.
Hosokawa Micron B.V. , Doetinchem, The Netherlands Hosokawa Micron B.V., located in the Netherlands, is specialised in Mixing, Drying, Agglomeration and allied Powder Processing Systems. The main activities are concentrated in the field of design and supply of equipment and systems for mechanical and thermal processing of dry and wet powders.
Hosokawa Micron is established in 1987, as a result of a merger between Nautamix Haarlem (founded in 1923) and Vrieco B.V. Zelhem (founded in 1939).
Constant efforts and improvements supported by Hosokawa Micron's intensive R&D programs, combined with many decades of practical field expertise, have led to a unique range of products which are continuously setting new standards in powder processing technologies.
The company's strong emphasis on system design capability is backed up by extensive test center and tolling facilities to support our customers in finding optimal solutions for their applications.
The sales programme of Hosokawa Micron B.V. includes the well-known brand names • Nauta • Schugi • Vrieco • Micron • ISEM
Humidity Technologies Pvt Ltd represents 'Condair' - a world leader in humidification. Product range includes industrial humidifiers and industrial dehumidifiers (solid desiccant dehumidifier) for various industrial applications like Pharmaceutical, Hospitals, Food & Confectionery, Automobile etc.
The company offers complete humidity solution from design to commissioning and after sales service.
Humidity Technologies Pvt Ltd is promoted by Shridhar Gokhale who has over three decades of experience in industrial Heating Ventilating & Air Conditioning (HVAC) with specialization in humidity control applications. The company is also supported by experienced application engineers from United Kingdom.
The company has built long term association with all customers by ethical dealings and offering the right technical solution from the wide range of products available. Some of our customers in India are - Lupin Limited , Cipla Limited , Sun Pharmaceutical Industries Ltd.etc.
Hyde Engineering + Consulting is a global design and consulting organization providing process system design, commissioning and validation, FDA compliance, and state-of-the-art cleaning technologies to pharmaceutical, bioprocess and other regulated process industries for two decades.
Headquartered in Boulder, CO, with offices located throughout the United States, Europe and Asia, Hyde has consistently been a leader in engineering, commissioning and qualification of equipment and clean utility systems. Due to its global capabilities, Hyde is able to provide clients the convenience of a single worldwide partner. Throughout the last 20 years, Hyde continuously strives to provide customers with current and relevant solutions that comply with the latest regulatory environment.
Our staff of over 200 professionals are dedicated to understanding the client's needs and exceeding their expectations.
Our experienced and knowledgeable staff will help you:
Reduce cost of goods
Add new product lines
Optimize cleaning cycles
Create product line extensions
Regardless of the size of the facility or complexity of the project, Hyde provides peace of mind through global expertise.
The Infionic Product Suite was launched in 2011 and since then we have had an ever growing customer base across US & India with our focus industries being Pharmaceuticals, Manufacturing and Professional Service Automation. With a steady pipeline, we anticipate significant growth in the current financial year across our target industries.
Our core activity is preparation of DMF / dossiers / CTD / COS / GMP / eCTD. We provide comprehensive solutions for preparation, filling and registration and updates of drug master files (DMF) for API and registration dossiers for formulations. We are an expert in CTD / ACTD dossiers for formulations. We have expertise and experience in preparation, filling and successful registration of COS or DMF for APIs, excipients and packaging materials. We also undertake bioequivalence/toxicity and Phase II III and IV clinical study projects. We also undertake technology transfer projects for finished formulations and APIs.
K A Malle Pharmaceuticals Ltd is an Export House and a leading manufacturer of API's, Drug Intermediates, Specialty Chemicals and Hydrogenation.
We are the largest manufacturers of Mebendazole (all grades) globally and one of the largest manufacturers of Albendazole in India. We are the pioneers of hydrogenation. We undertake contract manufacturing of almost all MNC`s and reputed pharmaceuticals companies of India.
As a partner of the international pharmaceutical and biotech industries we have a holistic approach to meet the process, production and packaging challenges of a regulated industry in a complex market.
Our aim is to provide added value and contribute to our customers success. With our 1,600 skilled and dedicated employees around the globe, and our integrated portfolio of machinery, software and material we offer solutions and services that perfectly fit our needs. This includes standard applications out-of -the-box as well as complex line concepts - all from a single source. To keep you focused on your core business.
Medipak Systems is partner to the international pharma and biotech industry with locations in Europe and around the globe.
We offer solutions for safe and efficient processes for the manufacturing, inspection and packaging of pharmaceutical products: including Pharma Manufacturing Execution Systems (MES), the development and production of standard and special folding boxes, innovative inspection and packaging machines and solutions for the traceability of medicines.
Medipak Systems unites the companies Dividella, Mediseal, Rondo, Seidenader Maschinenbau and Werum IT Solutions. Worldwide 1,600 employees work for our companies. Medipak Systems is the Pharma Systems business area of the international Körber Group.
multi-function group with over 40-year experience, millions of containers
manufactured for many among the most important brands in the pharmaceutical
industries worldwide. The Lameplast Group provides complete, flexible and
integrated services for manufacturing, filling and packaging of pharmaceutical
products and medical devices, from the empty containers to the finished
products, in single-dose, bottles and preservative free bottles. Exclusive
services: Pentafill Filling & Sealing Machines for single-dose plastic
containers; a new products portfolio with a complete line of CE Marked Medical Devices
ready for the market.
Leistung reaches various segments like food, pharma, beverages, cosmetics, bioscience, water treatment, dairy, healthcare & chemical.
Leistung has achieved numerous certificates like U stamp, UM stamp, R Stamp, NB Stamp, CE marking, US FDA, USP Class VI, ISO and many more.
Leistung's product range fall broadly in two categories namely:
LGC is an international life sciences measurement and testing company. Operating from state-of-the-art facilities to GLP, GCP and cGMP standards, LGC has leading capabilities in CMC, with particular specialties in materials science and pharmaceutical analysis. In support of the development and manufacturing of small and large molecule drugs, LGC provides method development, ICH validation and routine testing services. We offer unknown impurity determination, structure elucidation, compatibility studies, stability storage and testing. We are a leading provider of extractables and leachables studies and elemental impurity analysis. Our World-class material characterisation capability supports formulation development and manufacturing. LGC also has a state of the art bioanalytical capability in high-integrity analytical science and expertise spanning small and large molecules, biomarkers and molecular biology.
Malladi Drugs & Pharmaceuticals Ltd is an India based manufacturer of Active Pharmaceutical Ingredients (API). We have a strong global presence in the consumer health and generic market supplying to many of the large pharma companies across the globe. We are also involved in manufacturing of advanced intermediates, custom synthesis and contract manufacturing. Our facilities are FDA approved and we hold an eugmp as well.
Metina is a pharmaceutical consulting firm having expertise in submissions and approvals for USA, EU and Emerging Markets and expertise in filing & approval of ANDA, NDA, NCE as well as Branded Generic Products across the globe. Metina currently offers consultancy services to Pharmaceutical Industry and covers end to end regulatory and business development activity covering strategy development, due diligence of dossier, in-license/out-license of dossiers, Submission Management to Health Authorities, product market launch. It also offers consultancy services for EU GMP approvals, API QP Audits to the manufacturing sites in India and Worldwide.
Next Wave (India) is a WHO-GMP approved Pharmaceutical company. The company has state of the art facility to manufacture non betalactum finished dosage forms of Tablets, Oral Liquids, Capsules and Gels, Ointments & Creams.The company is reputed CDMO with independent facility to develop new products as per regulatory requirements. The company offers manufacturing capabilities for Indian and Global markets and has its own presence in various countries of SEA, LATAM and Africa region.
OMPI is part of the Pharmaceutical Systems division of Stevanato Group and boasts a unique expertise in providing superior pharmaceutical containers from glass tubing. With operations in Italy, Slovakia, Mexico, and China, Ompi offers the widest range of glass primary packaging, from the traditional ones such as vials and ampoules to the high-value ones as syringes and cartridges for auto-injectors and pen-injectors. Vials, cartridges, and syringes are available also sterile and ready to fill (Ompi EZ-fill®). pharma.stevanatogroup.com
Osmopharm SA is a Swiss pharmaceutical contract manufacturer specialized in the development and production of modified release solid oral form drugs. Osmopharm SA is GMP certified by the Swiss health authority Swissmedic, certificate with European validity thanks to the mutual recognition agreement between EU and Switzerland in accordance with quality and good practices defined by PIC/S (Pharmaceutical Inspection Convention/Co-Operation Scheme). With more than 150 formulations developed, the production capacity reaches 36 tons/month of nonsterile products in solid multi-dose form (controlled release granules) and unit dose form (controlled release tablets and capsules). Products: pellets, capsules, tablets in bulk and final packaging.
Pharmaffiliates Analytics & Synthetics (P) Ltd, is an integrated CRO (Contract Reserach Organisition) established in year 2005. Presently we are US-FDA accredited Facility We are specialized in research via synthesis of complex and difficult to make compounds, innovative organic molecules to support and accelerate the drug discovery research of pharma and biotech companies. We adapt unique synthetic approaches and execute in robust ways for making complex and unknown impurities with their characterization data. Thus we make the drug discovery process more efficient, cost-effective while maintaining the highest standards of quality. With the collective efforts of our team of 130 scientists so, far, we have performed more than 300 method validations & many of these validation reports submitted to EU & US & sought approvals. Work is carried in line with the ICH and the GMP guidance.
Our experience, combined with state-of- the-art laboratories and manufacturing facilities lets us become an ideal partner for the pharmaceutical and drug discovery industry , we undertake projects for process research, scale up , Custom Synthesis, CRAMS, Impurity synthesis, Isotope labeled compounds (Deuterium Compounds) ,Chiral compounds,Phytochemicals,Glucuronides, Reference Standards, Polymorphism studies, Analytical Method Development & Validation, Stability studies & Evaluation are of our core group activities. So far we have successfully established a library of more than 30000 compounds with their complete characterization data.
Your Complete Quality Solution Provider for the Life Science Industry. From registration to manufacturing and distribution, PQE is your global consultancy partner for quality and excellence. Your Expert in Full Data Integrity Assurance. Our broad services portfolio, extensive experience, effective project management, and exceptional cost effectiveness, have already proven to be a winning combination for global corporations, as well as small and medium sized companies. We are a UNI EN ISO 9001:2000 certified company with global capabilities across the whole product quality life cycle, allowing us to offer services at a very competitive price.
Revacure has a state of the art Oncology Injectable Formulations (Anti-cancer)manufacturing plant on a 12500 Sq. m plot at AKVN Industrial Area, Jabalpur. The company is having a complete technical support from world renowned pharma consultancy cGMP Pharma 'n' Plans Pvt Ltd for Design, Engineering, Qualification, Validation, on-going GMP Compliance, Quality Assurance, Training and Internal Audits. The Plant is WHO-GMP certified and the EU-GMP audit is scheduled in Jan 2018.
RGS is a company specialized in the manufacture of Industrial Vacuum Cleaners, Centralized Vacuum Systems and Pneumatic Conveyors for dust and granules.
With twenty years of experience in the area of automated industrial cleaning and the top competency of the technical staff, sales and post-sales, RGS Vacuum Solutions has consistently innovated, enhanced, and added its range of products by customizing each item according to the need and client requirements.
Shanghai Rich Chemicals Co Ltd founded in 1995, is a privately held chemical industry group company. With a strong focus on the development of high purity, high performance products and services for its high technology customers, demand has dictated expansion of its services, production and support to a global capacity. The company is recognized for innovation, technical expertise, revolutionary service and an unwavering commitment to safety and the environment.
Shanghai Rich Chemicals include the product such as Calcium Hypophosphite, Phosphoric Acid, Potassium Metaphosphate, Trisodium Phosphate, Disodium Phosphate, Monoammonium Phosphate, Monocalcium Phosphate.
Signet : Sourcing the world's finest excipients for the Indian pharmaceutical industry
For over twenty five years, Signet has aligned its key focus towards providing the world's best pharmaceutical raw materials to Indian scientists and formulators. By steadily establishing brands, promoting advanced processes and encouraging a shift towards newer developments and innovative applications, today Signet occupies a stellar position as India's largest excipients distributing company.
SimSon Pharma Limited, is one of the leading Manufacturer and Supplier of Pharmaceutical Reference Standards, Drug Working Standards, Drug Impurity Standards, Metabolites and Stable Isotope Labelled Compounds. We are pioneer in manufacturing Complicated Drug Impurity Standards and provider of complete solution in Identifying, Synthesizing and Qualifying any Unknown Impurity with more than 20,000 products ready in stock to ship. We are having our own Lab in Hyderabad, India wherein we specialise in below products & services.
are taking this opportunity to introduce our self as India's Leading
Turnkey Solution provider for Injectable Facilities for GENERAL
INJECTABLES, CEPHA-BETA, HORMONES, ONCOLOGY, VACCINES etc.
Our Consultancy Services includes…
Basic Facility Designing
Electrical and Civil
Designing & capacity calculations for equipment/systems
Floating of tenders
DQ approval, including drawings and layouts Inspection/FAT/SAT of equipment/system
Technical support during installation and commissioning
We specialize in the manufacturing of Complete Compact Lines For:
Vial Liquid with Lyophilizer with Auto loading and Unloading System
Ampoules with Automatic Inspection
PFS Filling- Plunger Rod Insertion- Labeling
Dental/ Insulin Cartridges
Nasal/ Mouth Spray (Sterile or Non sterile)
3- piece- Eye/Ear Drop Filling
Powder for Suspension Filling Lines
Combi Lines- Dual and Triple
Isolators for OSD & Aseptic Production Lines
Sterility Test - Dispensing – Formulation & Compounding
Snowbell provides solutions right from…
Infeed from decartoning with Inspection- Washing- Sterilizing & Depyrogenating Tunnel- Filling Machines- Auto Lyo- Loading Unloading System- Capping- External Washing- Auto Inspection- Labeling with integrated features of ORABS-CRABS-Isolators, Servo Based Check Weighing, with production rate from 25 to 500 Containers/min while incorporating the latest technology, conforming to the prevalent USFDA, MHRA, ENVISA, ENVIMA, EU norms
We are equipped with full-fledged manufacturing capability including state of art inspection facility to ensure standardized quality of all parental machines & equipment manufactured.
SPC is a dynamic chemical synthesis company associated with the pharmaceutical and lifesciences industry.
Delivering value through a combination of research and synthesis in a trusted and transparent manner, has made SPC a partner of choice among its customers and stakeholders seeking sourcing projects for intermediates and APIs.
Manufacturer and supplier of industrial chemical like cyclohexylamine, sodium metabisulfite
We are an expanding European manufacturer
founded in the Lake Como area in 1989, highly specialized in
the production of complete lines for the aseptic processing of
injectable products, supplying pharmaceutical companies worldwide.
We are focused on the development and production of highly technological and distinct solutions based on advanced engineering, providing tangible added value to customers looking for strong specificity combined to consistent quality.
Our approach is based on building a close partnership with our customers, where dialogue is frequent, open and ongoing at all stages of product lifecycle, to provide the most effective responses to clients' needs and the highest reliability in the long term.
SUSHEN is a global pharmaceutical project management services company promoted by a team of highly qualified and experienced international pharmaceutical experts. SUSHEN's range of services covers right from conceptualization and designing of a new plant, as well as existing plant, to its construction, and also setting up manufacturing facilities to its commissioning. The company's expertise also includes modification or extension of an existing plant with all modern and regulatory aspects. In short, we provide a complete turnkey solution for the pharmaceutical industry, under one roof.
Suven Life Sciences provides services to leading Global Life Science and Fine Chemical majors in the domains of Custom Synthesis, Process R&D, Scale up and Contract Manufacturing of intermediates, APIs and formulations, as part of its Contract Research and Manufacturing Services (CRAMS).
Since its founding in 1989, Suven Life Sciences has established its core competency in the development of small nitrogen containing Heterocycles such as pyrimidines, purines, indoles, and imidazoles. Adding to its renowned expertise in cyanation, Suven has also demonstrated its proficiency in Carbohydrate and Chiral chemistry including pyrroles, tetrahydrofurans, pyrans, amino acids and sulfoxides.
Suven's ability to collaborate on projects at all stages, from route scouting and development at gram scale through to commercial manufacture at multi-ton scale, provides a consistent and reliable partner throughout a product's life cycle and adds value through reduced transition times and tech transfer costs. Suven has two FDA approved cGMP facilities staffed with highly skilled and experienced teams, to meet the regulatory needs of our customers, from Advanced Intermediates to APIs.
Suven Life Sciences is a premier, fully integrated service provider to both Pharmaceutical and Chemical industries, worldwide. Suven has steadily demonstrated the ability to effectively use Its expanding infrastructure in order to contribute to the success of our clients at a different of stages of the drug development process, including the capability to reduce transition times and costs. Suven is dedicated to going beyond commitment and deliver R&D and Manufacturing solutions, with flexibility, quality, speed, and cost effectiveness, through our Contract Research & Manufacturing Services (CRAMS), Drug Discovery & Development Support Services (DDDSS) and Formulation Development Service. These capabilities and dedication have directly resulted in an impressive register of repeat clients, which include leading Global Life Science Majors and top Fine Chemical Companies.
Suzhou Highfine Biotech Co Ltd (HighFine) is an independent and technology-based company specializing in the production of diverse biochemicals and fine chemicals, especially peptide reagents and the related products. Facing the development trend of unifying global economy and that of growing regional economies, we will stand before the same milestone so as to cultivate a prosperous development, and we will work hard to upgrade people's health and our living standard. With the expert staff, advanced management and full access to state-of-the-art facilities, such as NMR, IR, Chiral & HPLC and so on, Highfine possesses the powerful research and development capability for new products, and assurance of product quality. Our goal is to reduce the cost and give the entire technique support and the best service for our customers.
Swiss Parenterals Limited, is a progressing dynamic pharmaceutical manufacturing company in India. We manufacturer Tablet / Capsules / Injections / Sterile Eye Drops / Syrups / Ointments etc. We have 3 Manufacturing Units and having accredation like TGA-Australia, Ukraine Pic/s, EU GMP (awaited) and many more. We introduce now Veterinery as well as Neutracutical range of products into our Business portfolio.
We manufacture Antibiotic / Antiulcer / Anasetatia / Antifungal / Analgesic / Laxatives / CNS-CVS etc.
Vanrx Pharmasystems makes the most technologically advanced aseptic filling solutions for the pharmaceutical industry. Vanrx pharmaceutical filling machines use robotics, machine vision and gloveless isolator technologies to automate the packaging of injectable drugs into vials, syringes and cartridges. The company was founded by pharmaceutical industry veterans to create the systems needed to make the next generation of innovative therapies. For more information, visit www.vanrx.com.
Viwit Pharmaceuticals Limited (Viwit), founded in 2006, is a fast-growing research-based pharmaceutical healthcare company dedicated to the development, manufacture and marketing of innovative products in the fields of Finished Dosage Formulations, Active Pharmaceutical Ingredients and Fine Chemicals. Viwit manufactures all the products based on company's core technologies, and is dedicated to serve customers for their greater success and healthier living. Viwit consists of six subsidiaries, including two integrated R&D centers and three cGMP production facilities. It covers a land area of 199,000 ? and employs nearly 500 staffs, including more than 150 scientists, many with PhD or master degrees. All three production facilities are managed under cGMP and ICH quality systems, and are certified respectively by cFDA (Chinese GMP 2010), ISO9000:2008, Mexican COFEPRIS, and World Health Organization. With mission statement of "Innovation for a better life" and culture of "integrity, respect, collaboration and excellence" at heart, Viwit is striving to become a global leading pharmaceutical healthcare company in the development and commercialization of specialty value-added products. Viwit creates values for customers, employees, shareholders and society, and contributes for a healthier and better world.
Willy A. Bachofen founded the company in 1933. He skilfully managed the difficult times during and after World War II and transformed the simple trading and manufacturing business into an industrial enterprise. In the early 1960s, the TURBULA®, the three-dimensional shaker mixer, and at the end of the 60s, the DYNO®-MILL, the first agitator bead mill with completely enclosed horizontal grinding chamber were successfully introduced worldwide.
Actions specified by Willy A. Bachofen were implemented on the occasion of the company's 65th anniversary to maintain the independent nature of the enterprise and to secure its jobs in the long term. Ultimately, these actions also benefit our customers and agents. To safeguard the future of the company and maintain its independence, shares were therefore issued to company employees from all units via a foundation. In employment, staff members have the rights and duties of a shareholder, but have to return the shares to the foundation when they leave the company.
The Company was established in 1988. Our major business is API production and CMO business. Our the major products are:- Naproxen, Naproxen Sodium, Acyclovir, Valaciclovir HCl, Clopidogrel isulfate/Besylate, Ganciclovir, Valganciclovir HCl, Famciclovir etc. The site has been inspected and approved by both US-FDA and EDQM.
Established in 1998, formerly called Jiacheng-Chem Enterprises, and in 2014, it was renamed to Zhejiang Eazy Pharmchem. We are your valued partner in Pharmaceutical intermediates, Active Pharmaceutical ingredients (APIs), and fine chemicals and in both R&D and commercial quantities. With experience of more than a decade in devotion to developing, manufacturing, sourcing and exporting to serve high quality products, Zhejiang Eazy Pharmchem keeps pace with the forefront of this constantly changing industry.
Zhejiang Jiuzhou Pharmaceutical Co Ltd is a medium-scale private enterprise and public company, which focuses in the production of APIs, Intermediates and contract manufacturing. We have four sites and two R&D centers. Our turnover of year 2014 is around USD208 million.
Products: Active Pharmaceutical Ingredients, Pharmaceutical intermediates