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GB United Kingdom
Stand No: 61D32
BDD is a specialist drug formulation company providing expertise across all areas of drug delivery. We offer a full service package to fit individual needs from troubleshooting, formulation development, in vitro and in vivo testing and full technology transfer. Our patented delayed release technology OralogiK provides unrivalled control of drug release at the right place and time. Our clinical division provides a full clinical package, including protocol development, study documentation design and regulatory authority submission, through to close out and production of ICH GCP-compliant clinical study report. We specialise in gamma scintigraphy, a powerful and versatile technology used to investigate the in vivo behaviour of your formulation. Coupled with pharmacokinetic data, this technique can be used to provide information on time /site of disintegration, gastric emptying, GI transit and intra/ inter individual differences.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
BioFilm has established an excellent reputation for developing and manufacturing thin dissolvable films (TDF) which release active ingredients. A range of actives can be incorporated into the films and the products can be classified as nutritional supplements, cosmetic, dental, medical devices through to medicinal and pharmaceutical. In fact, we produce more products in TDF than any other European manufacturer. BioFilm can offer companies a true partnership which allow us to take innovative concepts right through from initial research to development, manufacture, packaging and final delivery to the retailer. Thus enabling partners to launch innovative products quickly and cost effectively. Contact us today to learn more to discuss potential collaborations.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
Established in 2011, CMAC is a world-class international centre for manufacturing research and training. Working in partnership with industry, its purpose is to transform current manufacturing processes into the medicine supply chain of the future. The approaches developed and adopted within CMAC have been established through close collaboration with industry and the support of its partners, which include GlaxoSmithKline, AstraZeneca, Novartis, Bayer, Roche, Lilly and Takeda. The CMAC National Facility offers contract research support to industries through the delivery of services within crystallisation (batch & continuous), process development, formulation, product/process analysis and advanced materials characterisation. We are working with a range of companies based within the chemicals, agrichemicals and food industries applying our expertise in crystallisation, PAT and high end analytical services to these fields.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
EPP is a GLP compliant Contract Research Organisation (CRO) assisting pharmaceutical companies with pre-clinical environmental sciences testing. We ensure the smooth and efficient registration of your products by following OECD guidelines and can provide bespoke testing as required. We specialise in GLP complaint testing in the areas of: · Ecotoxicology; aquatic, marine and terrestrial · Environmental fate · Fish metabolism studies · Controlled substances · Storage stability · Physico-chemical testing · NMR EPP can additionally support your pharmaceutical registration and QC testing processes by providing custom synthesis of rare or unusual (non-commercially available) analytical reference standards of metabolites, impurities or degradants which are comprehensively certified to GLP compliant standards including by the use of GLP compliant NMR (both qualitative and quantitative).
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
Fountainbridge offer a complete sourcing service. Custom synthesis for non commercially available products and a market search to source the optimum supplier. Supported by independent QC analysis to ensure high quality of products.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
NCIMB provides specialist microbiology, chemical analysis and biomaterial storage products and services to support clients in their quality control procedures, research and development projects, intellectual property protection and compliance with environmental regulations.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
Scottish Development International (SDI) is the main economic development agency which helps businesses tap into Scotland's key strengths in knowledge, high level skills, technology and innovation. From its network of offices across the globe, SDI's experts deliver a value added service to give companies access to this wealth of knowledge and resources, from which to develop and exploit innovative ideas. With extensive experience of helping foreign-owned companies grow their business internationally, SDI is your starting point for Scotland. SDI will be hosting the Scottish Pavilion with 10 Scottish companies showcasing the chemicals capability that we have in Scotland.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
Solid Form Solutions Ltd is a world leading contract research organization (CRO) providing the pharmaceutical industry with chemical development services. Your flexible partner of choice when managing risk and cost in drug development. Our work programmes include : Salt Screening, Co-crystal Screening, Crystallisation Screening, Polymorph Screening, Amorphous Screening, Batch Process Development, Custom Synthesis, Physical Properties and Developability Testing. Our aim is to be flexible, understand our client's requirements and deliver workable solutions. Whether our expertise is required to locate a synthetic route or tackle specific problems encountered during drug manufacture, Solid Form Solutions will provide an unrivalled service.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
Symbiosis is a contract pharmaceutical manufacturing organisation (CMO) that specialises in the GMP manufacture and sterile fill/finish of vials of drug product for clinical trials and low-volume commercial supply. The core strengths of the company include regulatory compliance, technical capability and operational flexibility. Specialist manufacture of injectables takes place in a purpose-built MHRA-licensed facility, enabling Symbiosis to handle products that require aseptic liquid filling or lyophilisation for a range of complex biologic or small molecule drugs. Offering fast access manufacturing slots and accelerated release of drug product, Symbiosis is ideally primed to service demand for small-scale, fast-turnaround while providing drug product manufacturing excellence and ensures regulatory compliance to the highest standards.
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
TEMAG Pharma has become a highly reputable MHRA approved reliable company manufacturing and supplying unlicensed medicines to Hospitals, Pharmacies, Pharmaceutical Wholesalers, Dispensing Doctors and Buying Groups throughout the UK and across Europe. Our product range includes: Liquids: Oral and Topical liquids Semi-solids: Creams, Ointments, Gels and Suppositories and Pessaries Solid Dose: Hard Gelatine Capsules, Powders and Gelatine Free Capsules
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 61D32
Tepnel Pharma Services is an independent Contract Research Organisation that supports the drug development pipeline at the Rx/Dx interface. With over 30 years of experience in supporting pharmaceutical, biopharmaceutical and biotechnology companies through the provision of outsourced cGMP compliant chemistry, manufacturing and control (CMC) and human genetics testing, Tepnel Pharma Services is positioned to provide CMC support for drug development, whilst also providing a companion diagnostic solution that addresses the requirements of personalised and stratified medicines. Our CRO pharmaceutical testing facilities are located in the UK, and are configured to ensure maximum efficiency from sample receipt through to report delivery.
Location:
Sub-event: CPHI