Experience

The team have direct experience in the pharmaceutical industries with a focus on validation services and GMP documentation. Our experience is broad and covers the following sectors:

• API
• Primary and Secondary Pharmaceuticals
• Medical Device
• Biotechnology
• Contract Research Organisations
• Radiopharmaceuticals
• Engineering Construction and Management

We have worked on projects ranging from a single item of equipment to the full validation of a new build facility and our client list spans small start up companies to blue chip companies. A critical element of the work we do involves the documentation and assurance of materials of construction.

At QVR we are constantly involved in preparation work, audit assistance and remediation work related to FDA & MHRA inspections and have an excellent understanding of the regulatory requirements.

QVR have a truly global experience and have worked in: UK, Ireland, USA, South America, India, Europe and Eastern Europe.

In addition to our pharmaceutical experience we also have a keen interest and awareness of environmental requirements. A key member of our team is a qualified Lead Auditor of Environmental Management systems and has recently completed a Postgraduate Diploma in Environmental Management at Stirling University.

We are also active members of the following Institutes:
Institute of Biology
Institute of Environmental Management & Assessment