BioReliance® Validation Services
Rely on Experience
Accelerate and simplify your path to market by letting our experts from BioReliance® Validation Services help you choose and conduct the appropriate validation services for your filters, assemblies and single-use systems for drug manufacturing processing.
Rely on our experience to avoid regulatory observations and delays in your drug approval process.
Our validation project managers possess intimate knowledge of global and local regulations and industry best practices to assist you in developing and implementing an appropriate validation strategy. We can help you determine what, how and when to test; upstream, downstream, or final fill.
Trust Our Global Services Network For:
- Bacterial Retention
- Chemical Compatibility
- Integrity Testing
- Extractables and Leachables
- Patient Safety Evaluation
- Regulatory Consultancy and Custom Study Design
Choose BioReliance® Validation Services:
- Proven expertise and deep knowledge of biopharmaceutical processing, process technology and regulatory requirements for global markets
- Technology leadership with almost 50 years’ experience designing, manufacturing, and implementing filtration for pharma/biopharma manufacturing
- Global standards and localized services, with laboratories in five major geographic centers providing expertise in your time zone and language
- Commitment to the latest filtration, single use and membrane technologies, proven methods and established protocols.
We partner with you to implement a compliant, robust and effective validation strategy.
Rely on experience and inquire online about BioReliance® Validation Services today.