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U.S. FDA GMP Implementation for a Manufacturer of a Novel Protein Platform

PCS has helped a U.S.-based manufacturer of a novel protein platform with full GMP implementation for it's manufacturing sites in the U.S.

The consultancy services were rendered over a number of years, including support for re-construction and setting up the manufacturing process - including tech transfer.

PCS assisted with (at least) the following activities for the client;

  • Supply an interim vice president corporate Quality Assurance,
  • Drawing up plans for the reconstruction of a facility,
  • Create a manufacturing strategy,
  • Supervising clean construction management,
  • Selection of contractors,
  • Budgets,
  • Equipment purchase,
  • Validation, qualification,
  • Quality system implementation and supervision.

Other support included mapping the full production process, drawing up a production schedule, developing the cell bank and liaising with the U.S. FDA as well as suppliers and clients worldwide.

Client showcase project image