October 2009/1

NextPharma Technologies Partners with CARBOGEN AMCIS in Alliance which combines Investigational Medicinal Product and Active Pharmaceutical Ingredient Services for Highly Potent Active Pharmaceutical Ingredients

Surrey, UK, 7th October 2009

Surrey, UK, 7th October, 2009 - NextPharma, the leading European provider of product development, contract manufacturing and cold chain and logistics outsourcing services to the pharmaceutical and biotechnology industries, is pleased to announce that it has entered into an agreement with CARBOGEN AMCIS, a pharmaceutical process development and Active Pharmaceutical Ingredient (API) manufacturing company, to provide customers with  seamless development services covering highly potent pharmaceutical ingredient (APIs) and Investigational Medicinal Products (IMPs) for clinical trials.

The alliance offers a complete range of services for customers for both APIs and IMPs from pre-clinical to Phase III clinical trials.  The joint services will result in reduced cycle times, costs and risk related to the delivery of customer development projects. Sean Marett, Managing Director, NextPharma Technologies, Product Development Services commented: “Our customers are continuously looking at ways to speed-up development and reduce costs; this alliance moves customers one step closer towards achieving these goals”.

IMP development services to be provided by NextPharma include pre-formulation, formulation design and optimisation studies, IMP analytical methods development and methods validation studies, manufacturing of IMP non-GMP batches for toxicology testing and of GMP batches for clinical trials, IMP process scale up and validation studies, IMP stability studies according to International Conference on Harmonization (ICH) guidelines, Clinical Trial Services including packaging, labeling, randomisation and distribution, and IMP QP release and regulatory support services (for dossier submission of the IMP).

Services to be provided by CARBOGEN AMCIS include API categorisation and or OEL establishment of APIs and Intermediates based on available toxicology data and chemical structure, API process research, process development, process hazards and calorimetric assessments, API analytical methods development, API analytical methods validation, manufacturing of API non-GMP batches (toxicology, pilot batches), manufacturing cGMP API, API process scale up, API stability studies according to ICH, API process validation, and  regulatory support (for dossier submission) of the API.

“This alliance offers considerable added value to CARBOGEN AMCIS customers” commented Charlie Johnson, CARBOGEN AMCIS, High Potency Business Manager, “It’s difficult to find reliable API production and IMP service companies in the high potency arena; this agreement eliminates that challenge for customers.”

NextPharma develops, manufactures, packages, and distributes a broad range of products and formulations for its customers from tablets and capsules to antibiotics, hormones and controlled release medicines. It  has an established leadership position in the high technology area of injectables manufacturing, with particular expertise in product development and manufacture of oncology medicines.

CARBOGEN AMCIS AC is a leading provider of drug development and commercialization services to the pharmaceutical and biopharmaceutical industries through all stages of drug development. The integrated services of CARBOGEN AMCIS provide innovative, timely and safe drug development solutions that allow customers to make the best use of their available resources.
 

Contact:

Franck Latrille      
Chief Executive Officer  
NextPharma Technologies Holding Limited
Tel +44 (0) 1483 479 120

Notes to Editors:

About NextPharma

NextPharma Technologies, headquartered in the UK and founded in 2000, is a world class outsourcing partner to the pharmaceutical and biotechnology industry.

We offer a full range of services from early phase product development, through clinical trial packaging (Phases I through III) to high volume commercial manufacturing. We are a world leader in lyophilization, sterile fill finish and pellet technologies and in specialist product manufacturing including cytotoxics, hormones, penicillins, cephalosporins and controlled drugs. Our sterile development and production offers a full range of drug delivery technologies including pre-filled syringes, vials and ampoules. Additionally we have significant expertise in paediatric drug formulation, development and manufacture.

We operate globally with seven product development centres, seven manufacturing plants and six temperature controlled storage and distribution sites across Europe and North America, supplying customers in North America, Europe and Japan.
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We have 1,200 employees dedicated to serving over 200 customers world wide and a customer base, which includes many of the world’s leading pharmaceutical, specialty pharma and biotech companies.

We have a proven track record in almost all pharmaceutical technologies and product forms and in addition to the specialist areas above have capabilities in solids, semi-solids, liquids, sprays and dry dosage form technologies.

All of our sites are either FDA inspected, in the process of upgrade for inspection or targeted for upgrade for inspection.