BioReliance Validation Services
Rely on Experience
Accelerate and simplify your path to market by letting our BioReliance Validation Services help you select, test and validate the filters, assemblies and single-use systems for drug manufacturing processing.
Rely on our experience to ensure you don’t encounter delays or regulatory observations.
Our local Validation Coordinators possess intimate knowledge of local regulations and industry expectations to assist you in developing and implementing an appropriate validation strategy. We can help you determine what to test, and when – upstream, downstream, or final fill.
Trust Our Global Services Network For:
- Extractables and leachables testing
- Bacteria retention testing
- Integrity testing
- Compatibility testing
- Patient safety evaluations
Choose BioReliance Validation Services:
- Proven expertise and local knowledge of biopharmaceutical processing, process technology and regulatory requirements for global markets
- Technology leadership with 40 years’ experience designing, manufacturing, and implementing filtration for pharma/biopharma manufacturing
- Localized services, with laboratories in a half dozen major geographic centers to provide expertise in your time zone and language
- Commitment to the latest filtration, single use and membrane technologies, proven methods and established protocols
- Scientific, regulatory, drug development and manufacturing and other resources of Merck, a leading provider of cutting-edge life science systems
We partner with you to implement a thorough, effective validation strategy. Rely on experience – inquire about BioReliance Validation Services today.