Skip to content
  • Clinical Studies
  • Pharma SOP’s
  • Pharma tips
  • Pharma Books
  • Stability Studies
  • Schedule M

Pharma GMP

Your Gateway to GMP Compliance and Pharmaceutical Excellence

  • Home
  • Quick Guide
  • Toggle search form

Tag: GMP facility

Health Canada

Posted on March 12, 2024 By digi

  Exploring Health Canada: Safeguarding Public Health in Canada Introduction Welcome to a comprehensive overview of Health Canada, the federal department responsible for ensuring the health and safety of Canadians. Health Canada plays a vital role in regulating and overseeing various aspects of public health, including pharmaceuticals, medical devices, food, and consumer products. A Brief…

Read More “Health Canada” »

GMP Guidelines

Pharmaceutical and Medical Devices Agency (PMDA)

Posted on March 12, 2024 By digi

  Exploring the Pharmaceutical and Medical Devices Agency (PMDA) Introduction Welcome to a comprehensive exploration of the Pharmaceutical and Medical Devices Agency (PMDA), a critical regulatory body in Japan dedicated to ensuring the safety, efficacy, and quality of pharmaceuticals and medical devices. A Brief History The PMDA traces its origins back to the enactment of…

Read More “Pharmaceutical and Medical Devices Agency (PMDA)” »

GMP Guidelines

European Medicines Agency

Posted on March 12, 2024 By digi

  Exploring the European Medicines Agency (EMA) Introduction Welcome to a journey into the world of the European Medicines Agency (EMA), a pivotal organization in the realm of pharmaceutical regulation and oversight. A Brief History The EMA was established in 1995 with the primary aim of evaluating, supervising, and monitoring medicinal products within the European…

Read More “European Medicines Agency” »

GMP Guidelines

Posts pagination

Previous 1 2

Menu

  • GMP Basics
    • Introduction to GMP
    • What is cGMP?
    • Key Principles of GMP
    • Benefits of GMP in Pharmaceuticals
    • GMP vs. GxP (Good Practices)
  • Regulatory Agencies & Guidelines
    • WHO GMP Guidelines
    • FDA GMP Guidelines
    • MHRA GMP Guidelines
    • SCHEDULE – M – Revised
    • TGA GMP Guidelines
    • Health Canada GMP Regulations
    • NMPA GMP Guidelines
    • PMDA GMP Guidelines
    • EMA GMP Guidelines
  • GMP Compliance & Audits
    • How to Achieve GMP Certification
    • GMP Auditing Process
    • Preparing for GMP Inspections
    • Common GMP Violations
    • Role of Quality Assurance
  • Quality Management Systems (QMS)
    • Building a Pharmaceutical QMS
    • Implementing QMS in Pharma Manufacturing
    • CAPA (Corrective and Preventive Actions) for GMP
    • QMS Software for Pharma
    • Importance of Documentation in QMS
    • Integrating GMP with QMS
  • Pharmaceutical Manufacturing
    • GMP in Drug Manufacturing
    • GMP for Biopharmaceuticals
    • GMP for Sterile Products
    • GMP for Packaging and Labeling
    • Equipment and Facility Requirements under GMP
    • Validation and Qualification Processes in GMP
  • GMP Best Practices
    • Total Quality Management (TQM) in GMP
    • Continuous Improvement in GMP
    • Preventing Cross-Contamination in Pharma
    • GMP in Supply Chain Management
    • Lean Manufacturing and GMP
    • Risk Management in GMP
  • Regulatory Compliance in Different Regions
    • GMP in North America (FDA, Health Canada)
    • GMP in Europe (EMA, MHRA)
    • GMP in Asia (PMDA, NMPA, KFDA)
    • GMP in Emerging Markets (GCC, Latin America, Africa)
    • GMP in India
  • GMP for Small & Medium Pharma Companies
    • Implementing GMP in Small Pharma Businesses
    • Challenges in GMP Compliance for SMEs
    • Cost-effective GMP Compliance Solutions for Small Pharma Companies
  • GMP in Clinical Trials
    • GMP Compliance for Clinical Trials
    • Role of GMP in Drug Development
    • GMP for Investigational Medicinal Products (IMPs)
  • International GMP Inspection Standards and Harmonization
    • Global GMP Inspection Frameworks
    • WHO Prequalification and Inspection Systems
    • US FDA GMP Inspection Programs
    • EMA and EU GMP Inspection Practices
    • PIC/S Role in Harmonized Inspections
    • Country-Specific Inspection Standards (e.g., UK MHRA, US FDA, TGA)
  • GMP Blog
Widget Image
  • Qualify HVAC Systems in Warehouses to Maintain GMP Storage Conditions

    Qualify HVAC Systems in Warehouses… Read more

GMP facility

  • Health Products Regulatory Authority – HPRA
  • Explain the role of GMP in preventing contamination and cross-contamination
  • Explain the role of GMP in preventing contamination and cross-contamination.
  • GMP Guidelines to Ensure Product Quality and Safety
  • Principles of GMP
  • Pharmaceuticals – Process Validation
  • About Validation
  • China Food and Drug Administration (CFDA)
  • Therapeutic Goods Administration (TGA)
  • Medicines and Healthcare products Regulatory Agency (MHRA)

Copyright © 2025 Pharma GMP.

Powered by PressBook WordPress theme