Pharma Validation



Validation/Qualification in the pharmaceutical industry is the documented evidence, with a high degree of assurance, that any pharmaceutical-related processes, systems (facilities, equipment, and software), GMP procedures, and analytical testing methods comply with acceptable specifications and regulatory requirements.


Apart from the regulatory obligations, pharmaceutical companies are subjected to rationalized, robust, and risk-based validation approaches to significantly decrease the errors, contaminations, defects, customer dissatisfaction, non-complaints, recalls, return, destruction, and expense of routine tests and analysis while increasing trust, high quality, standards, regulatory compliance, revenue and profit in the long run.


NACPT validation webinars cover the verification, qualification, and validation processes and systems aligned with Health Canada, FDA, and European health authority’s requirements to meet consistency, repeatability, and reliability standards for improved product quality, safety, and efficacy. The webinars also include Validation Plan (VP), Master Validation Plan (MVP) or Validation Master Plan (VMP), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Computerized System Validation (CSV), Cleaning Validation (CV) and Process Performance Qualification (PPQ) required to create validation projects for a typical cannabis facility.




Scope of employment


  • Students can avail the following job opportunities after attending these five webinars on the Pharma Validation topic:
  •  Equipment Validation  Specialist
  • Validation Engineer
  • Validation Associates
  • Production Personnel
  • Computer Validation Specialist
  • Front/Backend Development officer
  • Enterprise Software Specialist


Webinar outcomes


  • A thorough knowledge base and skill set is developed in the Pharma Validation area after attending these webinars.

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