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:Read more
- Full CQV support. Our consultancy covers all aspects of the validation lifecycle as they relate to facilities, utilities, equipment, CSV, plus cleaning and process -qualification.
- Time critical delivery. We have experience of scoping, managing and successfully delivering C&Q projects where the construction and commissioning of the facility and utilities largely drive the project timelines.
- Specialist expertise. We have vast, high calibre experience within our team which means we can place the right experts on your project tailored specifically for your needs.
- Resource plugging. If you have a specific gap in resource or knowledge within your team, we can provide embedded client resources.