Intertek is a recognised leader in third–party conformity assessment on industrial processes, good manufacturing practice, and total quality management. With an in-depth knowledge of the critical manufacturing processes and the code of GMP, together with an extensive international network of experts in the pharmaceutical industry, Intertek is able to help our clients to achieve conformance to GMP guidelines.

Intertek is your partner in Quality Assurance from Design Phase to Performance Qualification. Intertek will work closely with you to provide the most cost effective measures in attaining pharmaceutical GMP certification and a competitive edge in the market.

Clean Room Validation:

Pharmaceutical manufacturing facilities require highest standards of clean room conditions, free of dust, and microorganisms to a level acceptable to both local and International Regulations & Standards.

Intertek undertakes validation of clean rooms, in Asia, Americas and Europe, with unparalleled experience and expertise on a regular basis.  This in-depth and detailed process includes establishing defined control limits, developing monitoring programs and documenting all results for review, reference, and record.  As a partner to global retailers, manufacturers, and distributors, we enable our customers to set, meet and evolve their quality, safety and performance standards

Validation Services:

• GMP Conformity Assessment Programs

• Validation of Critical Processes

• Qualifications of Equipment and Installation

• Clean Room Validation

• GMP Education