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GMP — Good Manufacturing Practice Certification

Good Manufacturing Practice certification demonstrates that your production processes, facilities and controls consistently produce safe, high-quality products — essential for pharmaceutical, food, cosmetic and supplement manufacturers.

What is GMP?

GMP covers the systems and procedures manufacturers must have in place to ensure products are consistently produced and controlled according to quality standards — covering premises, equipment, personnel hygiene, documentation and traceability.
RBA Registrars conducts independent GMP audits against recognised international frameworks, giving regulators, retailers and consumers confidence in your manufacturing controls.
WHY PURSUE THIS

Benefits of GMP certification

Consistent product quality

Documented, controlled processes reduce batch-to-batch variation and product failures.

Regulatory readiness

Aligns your facility with expectations from health authorities and retail partners.

Consumer trust

An independently verified mark of manufacturing discipline and product safety.

Market access

Many distributors and retailers require GMP as a condition of supply.
STAKEHOLDER TRUST

Supporting the Sustainable Development Goals (SDGs)

SDG 3

Good Health and Well-being

SDG 12

Responsible Consumption and Production

SDG 9

Industry, Innovation and Infrastructure

“Good Manufacturing Practice is not paperwork, it is proof that quality is built into every batch.”
Sarah Okafor, Lead Manufacturing Assessor, RBA Registrars

Organisations that benefit from certification

Food
Cosmetics
Textiles
Pharmaceutical goods
Manufacturer of medicines
Other manufacturing
What we audit

What we assess for Good Manufacturing Practice

Our assessors evaluate objective evidence against each focus area below and record findings in a formal audit report.
01
Facility & Equipment Controls
Premises design, cleaning validation and equipment qualification.
02
Personnel Hygiene & Training
Gowning, hygiene practices and role-specific competence training.
03
Documentation & Batch Records
Batch manufacturing records and document control requirements.
04
Quality Control & Testing
In-process and finished-product testing against specification.

Ready to begin your GMP certification journey?

Tell us about your organisation and we’ll return a fixed-price proposal — no obligation.