Validation requires the rigorous application of systematic GMP structure to ensure that quality is maintained at every stage from development through production. It involves the commissioning and qualification of facilities, systems, equipment, products and processes using proven methods. It begins with setting out a clear Top-to-Bottom hierarchy between policies, procedures and protocols to design a program that is effective, supportable and manageable.
Founded in 1995, as a Commissioning and Qualification company, Pharmatech has decades of experience in providing clients with advice in the commissioning and qualification (C&Q) of process equipment, utility systems and facilities. Using proven C&Q models, Pharmatech applies tools to reduce program time and cost while managing compliance risk.
COMMISSIONING AND QUALIFICATION
ANALYTICAL METHODS, PROCESS, CLEANING AND COMPUTERIZED SYSTEMS VALIDATION