Exquisite Science, Exceptional Service –
From Research To Release

At iuvo BioScience, our goal is to help you achieve yours. Our expert team will provide strategic guidance from research to release, leveraging our preclinical testing experience in medical devices, pharmaceuticals, and ophthalmics to deliver exquisite science, develop valuable insights, and author flawless documentation. And we do it all with a commitment to service, treating every project as if it were our own.

At iuvo, we don’t stay on our side of the wall. We break that wall down to become an extension of your team, because that’s what true partners do. It’s why we’ve redefined the CRO category and created something new and better – PRO – your Partner Research Organization.



iuvo BioScience Acquires Oculos Clinical Research

Combined expertise and experience creates fully integrated, research to release, ophthalmic development services company.

iuvo BioScience, an industry leading R&D services company specializing in safety, microbiology, toxicology, and analytical chemistry testing for the medical device and pharmaceutical industries, announced today that it has added Oculos Clinical Research, a leader in ophthalmic clinical research, to its corporate organization.

See how Oculos expand iuvo's opthalmic capabilities.



"We came to the team at iuvo BioScience with the need to complete testing required for a regulatory submission. Our team required this testing to be expedited; performed over a weekend. The team at iuvo provided us with a rapid response and professional approach meeting both our timeline and providing us data that allowed us to complete our filing on time."

Kevin Bentley / Executive Director of Regulatory Affairs and Quality, LSI Solutions


Advisory Services

iuvo BioScience scientists have extensive personal experience with the successful development and registration of medical device and drugs. iuvo advisory experts can assist you in evaluating new assets, developing your medical devices and pharmaceutical testing strategies, manage unexpected issues, prepare safety assessments and critical regulatory documents. Finally, our team of scientists specializing in sterilization can provide consultation in your sterilization strategy, cleanroom design and issue management.

  • Biocompatibility testing strategy development for medical devices and summary reports 
  • Toxicology testing strategy development for pharmaceuticals
  • Issue management and safety assessments
    • Actives, impurities, leachables, ingredients, material, process and packaging changes
  • Preparation and quality check of preclinical sections of NDAs, INDs, Annual Reports
  • Due diligence evaluations prior to purchase of new products
  • Sterilization strategy and issue management
  • Cleanroom design and validation
  • Water system design and CIP
  • Antimicrobial and biofilm assessment
  • Equivalency assessments to validated master products (sterilization and reusable device validations)

For more information on our Advisory Services please contact Donna Ventura at This email address is being protected from spambots. You need JavaScript enabled to view it..