Meeting the requirements of The Food and Drug Administration and the Medicines and healthcare Products Regulatory Agency.

We have a team of engineers with expertise in the validation process for:-

• Clean room environments
• Process equipment
• Process services

We have an in depth knowledge of current best practice and computer validation to current Good Automated Manufacturing Practice standards.

We carry out the preparation, processing and implementation of Validation master plans, Validation plans, functional specifications, Installation qualifications and operational qualification. All tailored to suit your project requirements.

We also carry out supplementary project support services to compliment our activities such as Work Package Co-ordination and Project Data manual Preparation including the preparation of pressure vessel/relief registration packages.