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Providing the benefits of differentiating technologies to PCAS customers

PCAS's industrial structure consists of flexible "multi-sites" for industrial implementation which leads rapidly to R&D fine-tuning, kilo-lab and pilot development. The organisation covers customers' potential needs by proposing a range of services required to develop a molecule throughout the clinical phases up to industrial product launch.

cGMP sites  l  Biocatalysts site  l  ISO-9001 sites  l  Headquarter

PCAS internationnal deployment 

PCAS is supported by:

  • A laboratory team supported itself by an analytical one, equipped with modern analytical tools at all sites, capable of carrying out and defining the first few grams of a product.
  • Centralized sourcing and raw materials purchasing departments which handle over 1100 references.
  • An industrial production capacity which places PCAS among the leading players in the worldwide market. Five cGMP sites, frequently inspected by official bodies (Medecines agencies)offering systematic back-up possibilities and back integration of intermediates manufactured at the 3 ISO 9001 sites. Confidentiality as well as guarantee of supply is certified throughout the manufacturing chain. FDA inspection of sites is a requirement to sell molecules to the USA.
  • A Quality Assurance organization which guarantees site cGMP level by following carefully regulatory issues and a recognized system by official bodies such as the FDA, EMEA, AFSSAPS and Japanese PMDA (KIKO).
  • A multi-disciplinary division dedicated to regulatory affairs authorization, based at Expansia site (Aramon), working in close and constant collaboration with PCAS team's development and manufacturing, customers, worldwide agencies and a network of experts for optimising regulatory lead-times.