For all pharmaceutical contract testing, the laboratory will provide customers at all times with a service complying with the requirements of the Medicines and Healthcare Products Regulatory Agency (MHRA). The laboratory will follow the principles and guidelines of Good Manufacturing Practice as laid down in Directive 2003/94/EC (Human Medicines) and Directive 91/412/EEC (Veterinary Medicines)
For all work carried out under the scope of United Kingdom Accreditation Service (UKAS), the laboratories will provide customers at all times with a service complying with ISO17025:2017
It is the policy of Quality Control North West – Stockport to:
