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Pharmaceutical Equipment Validation (PEV) Ltd The provider of specialist validation services to the pharmaceutical, biotech and medical device industries. We specialise in the qualification of equipment, facilities and utilities and work to meet the requirements of the UK (MHRA), European (EMEA) and US (FDA) regulatory authorities. We are Subject Matter Experts (SMEs) in the validation of moist heat sterilisation and dry heat depyrogenation processes, including the qualification of autoclaves and ovens and Sterilise in Place (SIP) systems for fermenters and vessels. We understand the benefits of a risk based approach to commissioning and qualification inline with that described in ICH Q9 and ISPE guidelines. Our dedicated team of Validation Specialists have considerable knowledge and experience, are GMP trained and come equipped with industry standard GE test equipment. Our approach is to work closely with our clients to ensure their requirements are clearly understood and the objectives achieved in a cost effective and timely manner. Our Quality Management System has been subject to audit by our clients. We have helped clients in the UK, Eire and Scandinavia. Mission Statement PEV endeavour to bring success to their clients by creating a team of talented and satisfied employees, |
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