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 subscribe to a Risk Based approach inline with that described in ASTM guide E2500, which applies the
concepts and principles introduced in the FDA initiative, “Pharmaceutical cGMP for the 21st Century, A Risk-Based Approach“.
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 dedicated and talented team of engineers have considerable
experience and knowledge,
acquired from within the Pharmaceutical / Biotech industry or by working with associated equipment
manufacturers
We have 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,
dedicated to exceeding expectations, by 'working with the client '
and not just 'for the client'.
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