Good Manufacturing Practice (GMP) is that part of quality assurance which ensures that medicinal products are consistently produced and controlled for the quality standards appropriate to their intended use and required by the marketing authorisation or product specification. A team of (GMP) auditors inspect our premises every 2 years to ensure our compliance with the EU GMP guidelines.

Sciantec Analytical Services Ltd has been audited by the MHRA and is approved for the chemical and physical analysis of pharmaceutical samples and premixes to current guidelines (GMP compliant).