Skip to content
Pharmaceutical Guidelines
Quality Is Policy
  • Home
  • Quality Assurance
    • List of SOP for Pharmaceutical Quality Assurance
    • SOP on Handling of Incidents and Deviations
    • SOP on Change control
    • SOP on Training of Employees
  • SOP Format
  • Quality Control
    • SOP on Cleaning Validation
    • SOP on Analytical Report (AR) Numbering
    • SOP ON Receipt, Issue & Control Of Lab Chemicals
    • SOP for Qualification of Quality Control analyst
    • SOP On Safety In Quality Control Laboratory
  • Production
  • Microbiology
    • SOP on Preparation of Culture Dilution
    • SOP on Microbial Testing of Drain Water
    • SOP ON BIO-BURDEN OF PACKING MATERIAL
  • Maintenance
  • EDQM
  • Analytical Method Validation
  • Process Validation
  • Drug Regulatory Affairs
  • ICH
  • cGMP
  • WHO
  • Blog
  • Contact Us
  • Privacy Policy

Tag: Quality Control Laboratory

HPLC Troubleshooting Steps for Pharma

August 20, 2020 Admin Leave a comment

HPLC Troubleshooting Steps for Pharma.

Continue Reading →

Posted in: Quality Control Filed under: Pharmaceutical Quality System, Quality Control, Quality Control Laboratory

General Safety Rules of Quality Control Laboratory

July 30, 2020 Admin Leave a comment

General and specific safety Rules & instructions reflecting identified risk, should be made available to each staff member and supplemented…

Continue Reading →

Posted in: Quality Control Filed under: Quality Control, Quality Control Laboratory, Safety Rules

Working procedures in Quality Control Laboratory

Admin Leave a comment

Working Procedure for Incoming Samples received by a laboratory may be for compliance testing or for investigative testing. Samples for…

Continue Reading →

Posted in: Quality Control Filed under: Quality Control Laboratory, Registration and labelling, test request, Working procedures

Pages

  • Analytical Method Validation
  • Blog
  • cGMP
  • Contact Us
  • Drug Regulatory Affairs
  • EDQM
  • Home
  • ICH
  • List of ICH Quality Guidelines for Pharmaceutical Industry
  • Maintenance
  • Microbiology
  • Privacy Policy
  • Process Validation
  • Production
  • Quality Assurance
  • Quality Control
  • SOP Format
  • SOP List For Pharmaceutical Quality Assurance
  • SOP on Change control
  • SOP on Handling of Incidents and Deviations
  • SOP on Training of Employees
  • WHO

Tags

Analyst Qualification Antibiotic Potency Testing Audit Preparation CAPA Change Management System Cleaning Validation Compression Machine Data Integrity EU Audit Requirements FDA Warning Letter HPLC Calibration ICH Guideline ICH Q10 laboratory guideline Manufacturing Site MHRA Microbial Testing Microbiology Microbiology SOP Microbiology Techniques OOS Out of Specification Out of Trend Pharmaceutical Production Pharmaceutical Quality System Phase-I Phase-II Phase Ia Phase Ib production Production SOP QMS Qualifications Protocol Qualification  Steps Quality Assurance Quality Control Quality Control Laboratory Quality Control SOP Quality Management System SOP SOP for Qualification of Quality Control analyst Stability Study Sterile Pharmaceutical products Sterility Testing USFDA
  • Home
  • Quality Assurance
  • SOP Format
  • Quality Control
  • Production
  • Microbiology
  • Maintenance
  • EDQM
  • Analytical Method Validation
  • Process Validation
  • Drug Regulatory Affairs
  • ICH
  • cGMP
  • WHO
  • Blog
  • Contact Us
  • Privacy Policy
Privacy Policy
Copyright © 2018 - 2020 Pharmaguideline