Training package In Good pharmaceutical manufacturing best practices – Material Drive

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Description

A quality system that meets pharmaceutical regulatory requirements is an essential component of every good drug manufacturing process. Participants in this course will be familiar with the basic features of US good manufacturing practices, GMP-compliant quality management system, as well as recent developments in drug regulation. In addition to explaining the duties of employees in production, quality control and quality assurance services according to the requirements of GMP compliant documents and records. This course provides participants with the necessary qualifications and experience to train and develop staff, focusing in particular on the relatively recent subject of safety of pharmaceutical data and controls on important electronic data systems that require high quality and quality management concepts and applications in the GMP environment.

What Will I Learn?

  • Explain the importance of good manufacturing practices (GMP) to ensure patient safety and drug effectiveness
  • Apply US-compliant pharmaceutical standards to enhance the current pharmaceutical quality management system within their organization
  • Continuing research and application of current GMP requirements and updates from US agencies
  • Application of pharmaceutical data safety systems
  • Produce documentation compatible with GMP procedures and written records
  • Prepare for regulatory inspections, internal audit and supplier audits

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