Welcome to QVR Limited

We specialise in the provision of professional and field services to the medicinal healthcare industries and have over 35 years experience in the validation and documentation of pharmaceutical, API, medical device, biotechnology sectors.

A key service we offer is the provision of a Positive Material Identification service for healthcare equipment within the context of a full understanding of Good Manufacturing Practices.

We use the latest portable X-RF technology allowing complete flexibility of the service. This means an independent and non-destructive testing which can be completed in situ and as a fundamental part of your IQ testing programme.

Three levels of service offered:

• In situ testing of plant at your facility
• Test equipment rental to allow you to utilise your own manpower resource
• Specific review and report of site PMI requirements for your facility - more »

We are exprienced and flexible enough to provide a comprehensive service from a single item of equipment through to the verification of an entire manufacturing facility.

Why use a Materials Testing Service?

How many times have you asked a vendor/contractor to supply documentation which assures you that the materials of construction are as specified?

How many times have you been given an accurate and GMP acceptable response?

How much time has your validation/QA team wasted chasing paperwork?

Is a single piece of paper from a steel foundry or a Certificate of Conformance sufficient evidence to guarantee that your equipment is made of 316L?

What do you do about existing (legacy) systems where there is no possibility of getting back dated documentation?

Solution:

Reliance on supplier evidence is often insufficient. We test the equipment in situ and provide documented evidence which clearly identifies the materials of construction. We can test both new and existing systems with minimum disruption to your process and plant. We provide a full GMP compliant report.

In situ testing provides hard evidence and assurance that the as-built unit complies to your user requirement specification and regulatory requirements.
It is suitable for both new and existing (legacy) systems.