Analytical method Quality Auditing

Quality assurance (QA) and independent audit is critical in the pharmaceutical industry to assure reliability of the products, adherence to approved specifications, and conformation of current good manufacturing practices (cGMP) to regulation. Manufacturers must establish a quality control unit that is responsible for quality-related activities required by the regulations. Quality is determined by whether the firm complies with GMP requirements and makes scientifically justified decisions. Pharmaceutical companies are now taking a proactive stance with the new GMP Systems approach, more effective internal auditing and increased regulatory awareness throughout the company.

  • Pharmaceutical Manufacturing Environment
  • Quality Control
  • Analytical Instruments
  • Quality Management System (QMS)
  • Quality Management System (QMS)
  • Laboratory Control System

Related Conference of Analytical method Quality Auditing

November 09-11, 2017

4th European Biopharma Congress

Vienna, Austria
August 20-22, 2018

9th Asian Biologics and Biosimilars Congress

Tokyo, Japan

Analytical method Quality Auditing Conference Speakers

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