Validation

  To confirm the compliance of the technology systems and installations with the standards of current Good Manufacturing Practice (cGMP) and with the requirements for specific “User Requirements Specification” (URS), a comprehensive set of qualified documents, made on the basis of strictly regulated procedures and developed for a specific project, must be submitted.

  BERHORD A&D offers its clients assistance in conducting the validation, providing a comprehensive multi-level support in preparing the documentation at all stages of the validation, from the Validation Master Plan (VMP) and the certification of Design Qualification (DQ), to the complex process of equipment qualification according to the IQ / OQ / PQ protocols.