AVF Chemical Industrial Co., Ltd is a large holding company, with three production bases and several contract manufacturers. We are specialized in high-tech level Animal health products, including veterinary APIs and Vitamin D3.
Our production is strict to GMPs. With a professional Registry Team, we have obtained ISO Kosher Halal FAMI-QS and the registrations of EMEA and EPA. From developing, sourcing, manufacturing, quality control to delivery, AVF controls every stage with a professional management system to guarantee stable quality and safety and ensure to provide value-added products and services for our partners.
With 10-year experience, our products have been sold to Europe, America, and Asia etc more than 40 countries and region, and we have a good reputation in these fields. And we are looking forward to be with you on the way of development.
Avivia is an independent specialized pharmaceutical development company engaged in drug repositioning, repurposing and reformulation. We operate a hybrid business model combining CRO service activities with internal product development programs, whereby in both cases, we approach ‘development' as not just offering a technical solution but always part of a broader product-oriented strategy. Our CRO services comprises complex drug product development and analytical development with unique dissolution and excipient characterization platforms.
AXXO is a leading international supplier with a rich product portfolio covering a wide range of therapeutic categories including active pharmaceutical ingredients (API), intermediates, finished dosage forms as well as the latest development in the field of biotech production i. e. monoclonal antibodies (MAB).
Our international operating company would be pleased to offer you our custom-made services from developing, manufacturing and marketing APIs, finished dosage forms or registration dossiers to full health concepts like machinery & equipment for your own manufacturing.
We are present in the EU, in a huge number of the CIS
countries and in various South American and Middle East markets. Our product
portfolio embraces APIs as well as finished formulations. Our dynamic and
highly-motivated team is investigating, developing, producing and distributing
innovative pharmaceutical products. We are offering just-in-time delivery,
customized product parameters as well as registration assistance.
Our expertise consists in the development and
registration of pharmaceutical products with a special emphasis on
Biotechnology, Oncology as well as Generic Drugs.
Leading fine and specialty chemicals group, French based, Axyntis with its 350 employees offers a deep rooted technical experience. The fine chemicals division (380 m3 under cGMP), is split into four plants (all AFSSAPS and one FDA approved): Orgapharm is designed for key advanced intermediates and exclusive APIs; Centipharm for key intermediates and generic APIs; AllChem for key intermediates -electronic, agro; Synthexim for key intermediates for pharma. Orgapharm and Centipharm bring in addition R&D and Pilot capabilities. With a wide range of key technologies, Axyntis is a specialist for various products such as indoles, quinolines, resolving agents, quinuclidines, fluoro aromarics
The headquarter of AZ GROUP locates in National Health Technology Zone of Zhongshan City, Guang Dong Province, P. R. China. It covers an area of 35,000 square meters, with the convenient transportation of one hour from Hong Kong by ferry. As an international and US FDA cGMP approved company, AZ GROUP is a Sino-US joint venture integrates R&D, manufacturing, marketing and customer services, it has been dedicating to the career of human health since its establishment. The product of AZ GROUP includes Pharmaceutical Products, D-Cal Calcium Supplements, Nutraceuticals and Health Food. It has a variety of international advanced manufacturing & testing equipments and refined production technologies. Strict quality management system and the internationalized specifications have been established to ensure the product quality. Some of our products are US FDA approved and exported to the countries including U.S.A, Europe and Canada etc.
Azelis is a leading supplier of active pharmaceutical ingredients (APIs) and excipients for the pharmaceutical, veterinary and health care industries. We are GMP certified by both the MHRA and Bezirksregierung Düsseldorf and have the required authorisations for distribution of psychotropic drugs and for controlled substances. Our dedicated team of more than 65 specialists includes expert pharmaceutical formulators and flavour technologists to support your new product development. Our Applications Laboratories provide full evaluation capability for all topical healthcare applications. Our technical sales support teams, backed by unique sourcing and integrated delivery systems can help to drive up quality, while reducing costs.
Azidus CRO, based in Chennai, India. Conducts BA/BE studies (healthy volunteers and patients), clinical trials, clinical data management, pharmacovigilance and regulatory submission to the global drug regulatory agencies. 480 Bed & 13 ICU bed Clinical facility and bio-analytical facility with 24 LC-MS/MS and 3 ICPMS under one roof. Approved by ANVISA Brazil, inspected by USFDA, DCGI, MOH-Turkey, GLP-Poland, UAE, Chile Health Authority, submitted studies for Spain and Germany. Clinical Laboratory approved by CAP (College of American Pathologists) and NABL.
Azierta is a Science and Health consultancy firm committed to strengthening bonds between science and the business environment through the “Science to Business” concept. We provide services in the field of medicinal products, Medical Devices, cosmetics, food supplements and biocides, offering complete solutions throughout products' life cycle, from medical and regulatory support, to toxicology, manufacturing and distribution needs, market access and pharmacovigilance. We have collaborated with more than 300 clients in the European environment through a multidisciplinary expert team, always focused on results and taking into account the needs of our customers. Services: European Market Access Support Services, Full Regulatory Affairs Support, Dossiers action plan, GMP Compliance Status Assessment, Pharmacovigilance services, Bioequivalence studies aligned with all EU requirements, Analytical support, Support for EU drugs auctions/tenders, Search of customers and sales networks, European Compliance Support services, Characterization of toxicological impurities, ERA (Environmental Risk assessment).