GMP And Requirements Of Premises, Plant And Equipment

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About Course

In this course learn about the Good Manufacturing Practices and Requirements of Premises, Plant and Equipment for Pharmaceutical Products.

Documentation is an essential part of the Quality assurance system and shall be related to all aspects of Good Manufacturing Practices (GMP). Its aim is to define the specifications for all materials, method of manufacture and control.

Language: English

What Will You Learn?

  • Introduction
  • General requirements
  • Warehousing ,Production & Ancillary Areas
  • Quality Control Area
  • Personnel
  • Health, clothing and sanitation of workers
  • Manufacturing Operations and Controls
  • Sanitation in the Manufacturing Premises
  • Raw Materials & Equipment
  • Documentation and Records
  • Labels and other Printed Materials
  • Quality Assurance
  • Specification:-
  • Master Formula & Packing Records
  • Batch Packaging Records & Processing Records
  • Standard Operating Procedures (SOPs) and Records
  • Reference Samples
  • Reprocessing and Recoveries
  • Distribution records
  • Validation and process validation
  • Other Important procedures

Course Content

Good Manufacturing Practices And Requirements Of Premises, Plant And Equipment For Pharmaceutical Products

  • Part 1
    08:28
  • Part 2
    06:27
  • Part 3
    08:19
  • Part 4
    07:15
  • Part 5
    08:09
  • Part 6
    06:04
  • Part 7
    08:37
  • Quiz:

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