Archemis

Archemis is a Contract Development Organization for all CMC section

Participated at Bio/PharMOS-Bio/PharDOS 2006 

Objective : Meeting customers looking for outsourcing CMC, contract or consulting services

Profile : Archemis is a Contract Development Organization specialized in providing CMC process research and development services to the pharmaceutical and biotechnology industry.

Based in France (Lyon), Archemis employs 150 world-class scientists, delivering bespoke solutions to individual customer needs under certified quality standards and strict confidentiality.

Services include:

• From discovery to clinical trials: consulting services for CMC development
• Quick, small-scale synthesis for Drug Discovery Support
• Chemical and Biochemical process development
• Analytical development, method validation, stability studies
• cGMP batch manufacturing for Drug Substance
• Cytotoxic or highly potent product manufacture
• Physical characterizations and polymorphism studies
• Preformulation (salt screening, crystallization)
• Formulation development (oral, parenteral, inhalation, topical)
• Process safety studies...

Archemis is organised in such a way that appropriate teams and facilities can be rapidly assembled around each individual project entrusted to us. Clients include Biotech Discovery or Development organizations and Big Pharma from across Europe and USA.

The facilities of Archemis are supported by a comprehensive array of structural and physical analytical instrumentation while our custom-built, cGMP qualified, cytotoxic kilolab features levels of segregated air handling and barrier technology rarely found in the industry.

Activities

• contract pharmaceutical manufacturing
• primary manufacturing (APIs)
• secondary manufacturing or processing
• generic pharmaceutical products
• antibiotics or cytotoxic products
• small volume manufacturing
• high containment production facilities
• contract development services
• development manufacturing for APIs
• pharmaceutical development services (PDS)
• formulation development
• drug delivery systems or technologies
• quality control (QC) or QA
• analytical testing and batch release
• consulting services for outsourcing
• scale-up from pilot to commercial volume
• lyophilisation (freeze-drying) services
• process validation, safety and testing