Validation Services

Equipment Validation

Our Equipment Validation Services


At Velopi, we provide technically experienced Equipment Validation Engineers to qualify your equipment. This service allows you to complete your equipment qualification goals without compromising on your core business.

All GMP equipment requires some validation effort. Depending on the complexity of the equipment, this can range from simple Installation Qualification/Operational Qualification testing to full Computer Software Validation.
 


We can help you complete your equipment qualification by creating & performing the key deliverables; such as, Equipment Specification generation, URS/FRS, Validation Plans, CSV, 21 CFR 11 requirements, Validation Reports, IQ/OQ documents, equipment vendor co-ordination.

Velopi offer Equipment Validation Services to the Medical Device and Pharmaceutical Industries both nationally and globally. Our Equipment Validation Engineers can assist in the development and execution of tailored templates specific to your organisations needs, for example;

IQ/OQ/PQ
Master Validation Plans
Protocols and Reports

Computer Software Validation


Do you need Equipment Validation consultancy services? If so, we can help your organisation. Our experienced staff can provide equipment validation services.

With this work outsourced to Velopi, you can concentrate on your your core business.

WITH VELOPI, YOU CAN DO IT RIGHT FIRST TIME - EVERYTIME!


Contact us for further information on what we can do for your organisation.

Email: info@velopi.com

Phone: +353 (0)21 240 6250

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