Skip to Content
MilliporeSigma
HomeServicesTestingViral Clearance TestingStandard and Hybrid Clearance Services

Standard and Hybrid Clearance Services

Our user-friendly facilities allow you to perform your viral clearance study with transparency and support by using our standard or hybrid services

Booking time at one of our facilities to execute your viral clearance study offers an optimal combination of flexibility, productivity, and quality assurance. In a user-friendly setting featuring the latest technology, transparency, and your choice of standard or hybrid clearance packages, our team provides precisely the level of support you require in pursuit of your IND or BLA filing.

  • Private client suites and laboratories
  • Suite-to-laboratory real-time video streaming
  • On-site IT support
  • Customizable lab set-up to maximize workflow efficiencies based on your requirements
  • State-of-the-art instrumentation to ensure successful execution

Your choice of standard or hybrid clearance services

Our standard clearance services make it easy to remain in control as you execute your viral clearance study. You will have access to our team for virus inactivation, freeing you to perform needed chromatography and viral removal filtration (VRF) as you see fit. At any step our team will be available to provide troubleshooting, offer guidance, or support your regulatory needs.

With our hybrid clearance package, we can serve as your co-pilot for completion of your viral clearance study. Collaborate with our team at our facilities, choosing the steps you want to perform while leaving the rest to us. For example, you can handle VRF and then return to your facility to conduct other work while we complete the inactivation and chromatography. Your final report will be delivered to you with our QA sign-off to support your regulatory submission.

To learn how we can meet your unique clearance needs, use our reply form and get in touch today.

Request Information

Related Services
Bulk Harvest Release Testing
Whether you’re preparing for first-in-human clinical trials or scaling up for global distribution of a life-changing therapeutic biologic, our cGMP-compliant bulk harvest release testing services protect your investment at every step.
Final Product Release Testing
With all biologics released into global pharmaceutical markets requiring GMP testing of final product, we offer a wide range of assays and lot release testing services to help you demonstrate compliance with regulatory guidelines.
Single-Use and Filter Validation Services
Accelerate and simplify your path to market by using our BioReliance® Validation Services to select, test, and validate your filters, assemblies, and single-use systems for drug manufacturing and processing.
Related Product Categories
Filtration
Filter paper, cut disc membranes, syringe filters, filter plates, and centrifugal, vacuum, and pressure filtration devices for chemistry, life science applications, and analytical methods.
Analytical Chromatography
Discover our premium products for accurate results in HPLC, GC, Karl Fischer titration, & more. From trace analysis to safety equipment, we've got you covered.
Related Applications
Viral Safety Assurance
A critical aspect of mAb manufacturing, viral safety assurance relies on established “prevent, detect, and remove” principles. Learn how you can tailor them to your own production upstream and downstream.
Monoclonal Antibody Manufacturing
Monoclonal antibody manufacturing requires scalable solutions ensuring high therapeutic concentration and process safety for immunotherapy.
Gene Therapy Manufacturing
Gene therapy innovation requires integrated manufacturing, testing, safety, and compliance expertise from experienced partners.
Vaccine Manufacturing
From early phase development, through downstream purification to large scale vaccine production: learn more about vaccine process development and application expertise.
Protein Expression
Protein expression technologies for various expression systems supporting research, therapeutics, and vaccine production.
Sign In To Continue

To continue reading please sign in or create an account.

Don't Have An Account?