Good Manufacturing Practice

Good Manufacturing Practice is the part of quality management which ensures that products are consistently produced and controlled according to the quality standards appropriate to their intended use and as required by the marketing authorization, clinical trial authorization or product specification. Good Manufacturing practices conference aims at both production and QC. Current Good Manufacturing Practices (cGMP) is aimed primarily at managing and minimizing the risks inherent in pharmaceutical manufacture to ensure the quality, safety and efficacy of products. FDA regulates the quality of pharmaceuticals very carefully. Current Trends in the FDA is the main regulatory standard for ensuring pharmaceutical quality.

As per the current statistics, the country’s pharmaceuticals industry accounts for about 2.4% of the global pharma industry by value and 10% by volume. The industry revenues are also expected to expand and grow at a CAGR of 12.1% during 2012-20 and reach USD 45 Billion. Currently, the healthcare sector in India is USD 65 billion and is expected to grow to USD 250 Billion by 2020.

  • Facts About Current Good Manufacturing Practices (cGMPs)
  • Good Automated Manufacturing Practice (GAMP)
  • FDA Good Manufacturing Practices
  • GMP/GCP Interface & GMP audits
  • GMPs for Medical devices
  • GMPs for OTC and Cosmetic Products – Global Requirements
  • GMP Requirements & Standards

Related Conference of Good Manufacturing Practice

August 20-21, 2018

9th Asian Biologics and Biosimilars Congress

Tokyo, Japan
October 18-19, 2018

18th World Pharma Congress

Warsaw, Poland
September 18-19, 2018

6th European Biopharma Congress

Amsterdam, Netherlands

Good Manufacturing Practice Conference Speakers

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