QUALITY ASSURANCE (QA) DEPARTMENT

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About Course

QUALITY ASSURANCE (QA) DEPARTMENT – SYLLABUS :

  • Good Manufacturing Practice (GMP) , D & C Act – Schedule M .
  • Good Laboratory Practices (GLP) , D & C Act – Schedule L1
  • Role of Quality Assurance Department in Pharmaceutical Organizations  & 10 Principles of GMP.
  • Quality Management System (QMS)
  • Fundamentals of Standard Operating Procedures (SOPs) ,SOP

    Index/List & QA SOPs.

  • Good Documentation Practice (GDP).
  • QA In-process (IPQA) Checks on Pharmaceutical Organization.
  • Internal audits / Self Inspection / External Audits & Vendor Audit.
  • Change Control & Deviations
  • Site Master File (SMF).
  • Market complaint Investigations, evaluation & Corrective And Preventive Actions (CAPA).
  • How to face interview in Pharmaceutical organizations.
  • Important likely questions asked during interview in pharmaceutical

         Organizations.

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What Will You Learn?

  • QUALITY ASSURANCE (QA) DEPARTMENT - SYLLABUS :
  • • 1. Good Manufacturing Practice (GMP) , D & C Act – Schedule M .
  • • 2. Good Laboratory Practices (GLP) , D & C Act – Schedule L1
  • • 3. Role of Quality Assurance Department in Pharmaceutical Organizations
  • & 10 Principles of GMP.
  • • 4. Quality Management System (QMS)
  • • 5. Fundamentals of Standard Operating Procedures (SOPs) ,SOP
  • Index/List & QA SOPs.
  • • 6. Good Documentation Practice (GDP).
  • • 7. QA In-process (IPQA) Checks on Pharmaceutical Organization.
  • • 8. Internal audits / Self Inspection / External Audits & Vendor Audit.
  • • 9. Change Control & Deviations
  • • 10. Site Master File (SMF).
  • • 11. Market complaint Investigations, evaluation & Corrective And
  • Preventive Actions (CAPA).
  • • 12. How to face interview in Pharmaceutical organizations.
  • • 13. Important likely questions asked during interview in pharmaceutical
  • Organizations.

Course Content

QUALITY ASSURANCE (QA) DEPARTMENT ( 13 Videos)
QUALITY ASSURANCE (QA) DEPARTMENT - SYLLABUS : • 1. Good Manufacturing Practice (GMP) , D & C Act – Schedule M . • 2. Good Laboratory Practices (GLP) , D & C Act – Schedule L1 • 3. Role of Quality Assurance Department in Pharmaceutical Organizations & 10 Principles of GMP. • 4. Quality Management System (QMS) • 5. Fundamentals of Standard Operating Procedures (SOPs) ,SOP Index/List & QA SOPs. • 6. Good Documentation Practice (GDP). • 7. QA In-process (IPQA) Checks on Pharmaceutical Organization. • 8. Internal audits / Self Inspection / External Audits & Vendor Audit. • 9. Change Control & Deviations • 10. Site Master File (SMF). • 11. Market complaint Investigations, evaluation & Corrective And Preventive Actions (CAPA). • 12. How to face interview in Pharmaceutical organizations. • 13. Important likely questions asked during interview in pharmaceutical Organizations.

  • 1. Good Manufacturing Practice (GMP) , D & C Act – Schedule M
    15:58
  • 2. Good Laboratory Practices (GLP) , D & C Act – Schedule L1
    00:00
  • 3. Role of Quality Assurance Department in Pharmaceutical Organizations  & 10 Principles of GMP.
    00:00
  • 4. Quality Management System (QMS)
    00:00
  • 5. Fundamentals of Standard Operating Procedures (SOPs) ,SOP Index/List & QA SOPs.
    00:00
  • 6. Good Documentation Practice (GDP).
    18:51
  • 7A. QA In-process (IPQA) Checks on Pharmaceutical Organization.
    16:17
  • 7B . QA In-process (IPQA) Checks on Pharmaceutical Organization.
    00:00
  • 8. Internal audits / Self Inspection / External Audits & Vendor Audit.
    00:00
  • 9. Change Control & Deviations
    00:00
  • 10. Market complaint Investigations, evaluation & Corrective And Preventive Actions (CAPA).
    00:00
  • 11. Preparation and Implementation of Site Master File (SMF).
    00:00
  • 12. How to face interview in Pharmaceutical organizations.
    00:00
  • 13. Important likely questions asked during interview in pharmaceutical Organizations.
    00:00

QA SOP Drive Link
Click on this Link :- https://drive.google.com/drive/folders/1g8amUz9HE6JlStQoOSoffxp5kLSKXrqS?usp=sharing

QA SOP

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