Verisys has a team of experienced Validation Engineers available to meet the requirements of the Food and Drug Administration and the Medicines and Healthcare Products Regulatory Agency.
Validation has formally been defined as “the process of establishing documented evidence which proves a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality characteristics”. Although making direct reference to product manufacture, the definition lends itself in principle to any item of equipment or mechanical services which by its nature or function has the potential to impact upon product quality.
This validation service is offered to
- Process Equipment
- Process Services
We have an in depth knowledge of current best practice and computer validation software.
Verisys carry out the preparation, processing and execution of Validation Master Plans, Validation Plans, Functional Specifications, Installation Qualifications and Operational Qualification. These can be 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.
Speak to a specialist Engineer today by filling out the contact form or calling us on 0330 053 2218.
Why choose Verisys?
Verisys can be relied upon to provide a high-quality service from start to finish, even in the most demanding of environments.
tailored to your needs
Project management consultancy services
End to end commissioning services
High level of service