Validation

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 to:-

• Clean Room Environments
• Process Equipment
• Process Services

We have an in depth knowledge of current best practice and computer validation to current GAMP** standards.

We carry out the preparation, processing and execution of Validation Master Plans, Validation Plans, Functional Specifications, Installation Qualifications and Operational Qualification, all tailored to suit your project requirements.

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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.

**Good Automated Manufacturing Practice

 Validation PDF

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End Systems Limited
Redwater House, Brunswick Street, Leigh, Lancashire WN7 2PL
Tel: 01942 673229 / Fax: 01942 260155