Pharmaceutical Good Manufacturing Practice (GMP) Auditing and Good Clinical Practice (GCP) Auditing for equipment, facilities, utilities, processes and process installations.
Pharmaceuticals must be produced consistently and must be strictly controlled to meet both national and international standards appropriate for their intended use. Strict regulatory requirements must be met including those specified by US Food and Drug Administration (FDA) or UK Medicines and Healthcare Products Regulatory Authority (MHRA).
Our auditing team offer Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) audit services helping our clients to ensure that all relevant regulatory requirements (FDA, NF, MHRA) are met. We provide auditing solutions - including pharmaceutical shared audits - for all types of pharmaceutical products such as active pharmaceutical ingredients (APIs), drug products, excipients, over-the-counter products, vaccines and vitamins.
Intertek can add value to your business by helping you to achieve or maintain regulatory compliance for equipment, facilities, utilities, processes and process installations. Our global network of experienced auditors are available to conduct audits supporting the entire manufacturing supply chain.
Need help or have a question?
- N. America
- +1 800 967 5352
- +1 908 534 4445 x600
- EMEA UK:
- +44 161 721 5247
- +41 61 686 4800