cGMP

cGMP

cGMP stands for Current Good Manufacturing Practice. It is a system of regulations enforced by regulatory agencies like the U.S. Food and Drug Administration (FDA) to ensure that products—especially in pharmaceuticals, biotechnology, food, and medical devices—are consistently produced and controlled according to quality standards.

Current Good Manufacturing Practice cGMP in General

This standard integrates requirements for both products and processes within manufacturing operations. It also:

  • Ensures full compliance with national and international regulatory requirements.
  • Can be implemented in organizations of any size or structure, including multi-site setups.
  • Ensures ongoing improvement and efficiency in operations.
  • Identifies and controls risks and hazards in products and processes to ensure consumer protection.
  • Helps the organization maintain consistent quality and safety throughout the production lifecycle.

What we can do for you in cGMP Compliance?

  • cGMP Policy, Procedure & Documentation Templates or Customized Documents
  • cGMP Implementation Support and Expert Consultation
  • Internal Audit Services for cGMP Compliance
  • Independent cGMP Audit Coordination via Accredited Certification Bodies
  • Full-Service Package: Documentation, Implementation, Training, Internal Audit, and Certification Coordination

Get your cGMP Compliance Service Now

A team of ISO specialists, auditors, and industry experts dedicated to making certification simple, reliable, and effective. We support ISO Certifications and Global Regulatory Frameworks (MDSAP, MDR, FDA, TGA, MHRA), helping businesses meet international standards with confidence.

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