Good Manufacturing Practice

GMP Certification Consultants in UAE & Middle East

Ensure consistent quality and safety in your manufacturing processes. Expert GMP consultancy for Pharma, Cosmetics, and Food industries in India, UAE, and Saudi Arabia.

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Quality That Is Built-In, Not Tested-In

Mandatory compliance for regulated industries.

Good Manufacturing Practice (GMP) represents that part of Quality Assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use.

Unlike end-product testing, which can only find defects after they occur, GMP is designed to prevent mistakes like cross-contamination, mix-ups, and false labeling.

From WHO-GMP for pharmaceuticals to ISO 22716 for cosmetics, IQS helps manufacturers in India and the Middle East meet stringent regulatory requirements.

GMP Clean Room

The 5 P's of GMP Excellence

People

Training, hygiene, and clear roles.

Procedures

Documented SOPs for every task.

Products

Specs for raw materials & finished goods.

Premises

Lab layout, cleanliness, and HVAC.

Processes

Validation, calibration, and control.

Sectors Requiring GMP

Pharmaceuticals

WHO-GMP compliance for drug manufacturing.

Cosmetics

ISO 22716 standard for cosmetic products.

Food & Supplements

Essential for dietary supplements and processing.

Medical Devices

Quality system regulation for device integrity.

Our GMP Implementation Roadmap

We provide end-to-end support for implementing GMP in your facility, ensuring compliance with CDSCO (India), SFDA (Saudi Arabia), and MoHAP (UAE) regulations.

  • Gap Analysis: Detailed assessment of your facility vs GMP norms.
  • Layout Review: Consulting on facility design, flow, and HVAC zoning.
  • Documentation: Writing SOPs, Batch Manufacturing Records (BMR), and protocols.
  • Validation Support: DQ/IQ/OQ/PQ for equipment and utilities.
  • Mock Audits: Pre-audit inspections to ensure 100% readiness.
Pharmaceutical Manufacturing Audit

Why Choose IQS?

Pharma Experts

Our team includes former Quality Managers from top pharma companies.

Regulatory Insight

Up-to-date knowledge of US FDA, EU GMP, and WHO guidelines.

Integrated Systems

Seamlessly integrate GMP with ISO 9001 and ISO 22000.

Frequently Asked Questions

cGMP stands for *current* Good Manufacturing Practice. The "c" emphasizes that expectations are dynamic; manufacturers must use technologies and systems that are up-to-date with today's standards, not just what was good enough 10 years ago.

No. While pharmaceutical companies have the strictest requirements, GMP is also mandatory for small cosmetics manufacturers and food processors. The scale of implementation is tailored to the size and complexity of your operation.

Timeline depends on your current facility conditions. For a new facility designed with GMP in mind, it can take 3-4 months. For older facilities requiring upgrades and extensive validation, it may take 6-12 months.

Elevate Your Manufacturing Standards

Achieve WHO-GMP, ISO 22716, or Food GMP Certification.

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