QC & QA: Quality control and Quality assurance

With greater attention to the following elements this session will discuss the all the key lookouts essential for the development of a QA/QC system in pharmaceutical manufacturing process and requires implementation in tracking inventory compilation:

·         An inventory agency responsible for coordinating QA/QC activities;

·         A QA/QC plan;

·         General QC procedures

·         Source category-specific QC procedures

·         QA review procedures;

·         Reporting, documentation, and archiving procedures.

 Market research analysts predict that the global automated industrial quality control (QC)  market will grow steadily at a CAGR of around 8% by 2021.

  • ICH:International Council for Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
  • " Hazard analysis and critical control point (HACCP) methodology for pharmaceuticals"
  • WHO compendium of guidelines for pharma QA
  • Quality management system (QMS) in cGMP
  • Data Integrity in Pharmaceutical Quality Control Laboratories
  • GLP compliancing
  • cGMP compliancing

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