Qualification & Validation

In highly regulated industries such as pharmaceutical, biotechnology and life sciences, CQV is critical to getting your products from the laboratory setting through to market.

Regulatory requirements are constantly changing, and the need for maximising efficiency has never been greater. Yet despite the critical nature of CQV, many companies lack the in-house expertise and resource to undertake this sufficiently and so turn to specialist CQV consultants.

At Scitech, we have a large team of 50+ commissioning qualification and validation consultants available to provide guidance on all aspects of CQV. Our team holds extensive experience, knowledge and technical expertise developed over many years servicing the pharmaceutical, biotechnology and life science industries.

Our services span from audits in relation to CQV (including procedures, protocols, and data integrity), cost and timeline estimates for large new capital projects through to small work packages, ongoing embedded CQV support (short or long term), plus assistance with deviations, CAPAs, and FMEAs.

In accessing our specialist CQV consultancy services, you will benefit from:

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