• 0-9
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
  • J
  • K
  • L
  • M
  • N
  • O
  • P
  • Q
  • R
  • S
  • T
  • U
  • V
  • W
  • X
  • Y
  • Z
  • All
CECyC Pharma - Clinical and analytical research center with facilities in Mexico City. We specialize in: Bioequivalence Studies Clinical Trials Phase I - IV Interchangeability of drugs in vitro
FR France
Stand No: 41C50
A 25 years pharmaceutical company specialized in: - Clinical supplies: support to pharmaceuticals/biotech companies in their Phase I to IV clinical trials, from comparator sourcing to worldwide logistics, through primary & secondary packaging - Customized Manufacturing Operations: packing, repacking & distribution of drug products and food supplements, without minimal batch size
DE Germany
Stand No: 40C35
GBA Pharma is a service provider for pharmaceutical companies and is supporting research & development as well as services in the commercial stage. Our success and opportunities is based on a high qualified staff. The headcount of GBA Pharma represents 200 employees distributed over 5 locations in Europe with +50% academic staff. Our portfolio comprises the following service areas: Contract research in the preclinical arena (in vitro & in vivo) Pharmaceutical testing under GMP incl. stability study services & QP release services Bioanalysis under GLP: in vivo toxicology studies and phase-I/II clinical studies GMP qualification of API and drug manufacturer outside the European Union Distribution and clinical trial supply management for multicentre trials Consultancy & regulatory affairs with regard to GMP, GLP & GCP We would be delighted to develop a tailored solution for you.
BR Brazil
Stand No: 110A41
ICF has been founded in 2002 and it has been the first Brazilian bioequivalence and bioavailability laboratory to get certified by ANVISA (Brazil). It is one of the largest pharmaceutical research centers in Brazil and in Latin America and a notable reference for industries and investors from several countries. ICF's commitment with ethics and innovation assure the credibility and quality of our products. ICF has already conducted over 700 bioequivalence studies and it takes part in the history of generic drugs in Brazil. We offer one of the biggest hospital infrastructures in the country with a high technology, diversified portfolio and certificate, two hundred bioanalytical methods – including high complexity methods such as hormones and sprays.?
Sub-event: CPHI
Zone: API
DE Germany
Stand No: 41N04
As a partner for the industry, Navitas Life Sciences leverages industry insights, consulting and technology capabilities to deliver full service clinical, regulatory and safety solutions and desired outcomes to our clients. Navitas Life Sciences, the dedicated life sciences company of TAKE Solutions, harnesses the combined knowledge and experience of three legacy companies—Ecron Acunova, Navitas, and Intelent—to provide end-to-end services and solutions. We help our clients address their most critical problems by bringing together the capabilities of a full-service CRO, a technology-led life sciences services provider across clinical, regulatory and safety, and a life sciences big data services and analytics provider. With a rich legacy of experience in life sciences, we have worked with 9 of the top 10 global pharma companies.
IN India
Stand No: 41N44
Raptim Research Ltd. is a quality-oriented full-service contract (clinical) research organization. Raptim provides end-to-end services to global Pharmaceutical (generic as well as research-based), Biotechnology and Cosmetic industry. The studies done at Raptim are globally submitted and approved by various regulatory agencies including USFDA, EMA, UK MHRA, Canada (TPD), WHO and etc. Raptim Research Ltd., incorporated in the year 2005, has its facilities based in Navi Mumbai and Business Office in Navi Mumbai as well as New Jersey, USA. Raptim is leader following activities: Bioequivalence / Bioavailability Studies (BE/BA studies) PK end-point studies PD end-point studies Clinical trials – phase II & IV Studies on Special Population Apart from the above, Raptim has developed expertise in niche area of drug development and has pioneered in testing/screening Dermal Topical Products including Cosmetic Products as well as inhalation products. These include: In vitro Release/Permeation (IVRT/IVPT) studies In vivo – Tape Stripping studies In...
SE Sweden
Stand No: 41K10
Recipharm is a leading contract development and manufacturing organisation (CDMO) headquartered in Stockholm, Sweden. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and are continuing to grow and expand our offering for our customers. Employing around 5,000 people, we are focused on supporting pharmaceutical companies with our full service offering, taking products from early development through to commercial production. For over 20 years we have been there for our clients throughout the entire product lifecycle, providing pharmaceutical expertise and managing complexity, time and time again. Despite our growing global footprint, we conduct our business as we always have and continue to deliver value for money with each customer's needs firmly at the heart of all that we do. That's the Recipharm way. For more information visit www.recipharm.com
ES Spain
Stand No: 40D33
TECNALIA offers services and R&D across entire value chain(human medicines, medical devices, food supplements, cosmetics & veterinary medicines). • Pharmaceutical development:Galenic & Analytical Development, Analytical methods Validations, Stability Studies • Clinical Trials:Bioequivalence Studies, PhaseI,II,III&IV Clinical Trials, Nutritional Clinical Studies. • Manufacturing:Contract Manufacturing of Industrial Batches for Third Parties • Pharmacogenetics
DE Germany
Stand No: 41K70
Vetter is a leading contract development and manufacturing organization (CDMO) that specializes in the aseptic filling of syringes, cartridges and vials. The company has extensive experience with biologics and other complex compounds, including monoclonal antibodies, peptides, interferons and vaccines. Collaborating with pharma/biotech clients worldwide, Vetter supports products from preclinical development through global market supply. Through its U.S. and European facilities, Vetter Development Service provides state-of-the-art support for early-stage products, with seamless transfer at Phase III to Vetter Commercial Manufacturing for large-scale production. The company offers state-of-the-art technology and innovative processes to promote product quality and maximize API yield.
GB United Kingdom
Stand No: 41L08
The Wasdell Group provides the pharmaceutical and nutraceutical industries with solutions to a range of outsourcing requirements. Established in 1971, with multiple sites in the United Kingdom and employing over 600 people, the group offers an impressive range of technical, manufacturing, packaging and storage/distribution services. The Wasdell Group prides itself on delivering high quality, reliable, flexible and responsive services with unrivalled lead times.
DE Germany
Stand No: 40L52
World Courier is the most trusted, global specialty logistics company in the world. Our services and solutions include a global network of 140+ offices in 50+ countries and 14 depots, clinical trial logistics, temperature control solutions, GxP compliance and pharmaceutical storage and distribution
Sub-event: PMEC
Zone: PMEC