July 18, 2023
iuvo BioScience Hires Industry Executive to Lead Clinical Research Team
Exquisite Science. Exceptional Service.
From Research to Release.
Premier Partner Research Organization
Serving the Medical Device, Pharmaceutical, and Ophthalmic Industries
Our team of experts will provide the strategic guidance and testing services you need – from research to release. We can leverage our preclinical testing, CMC/technical services, and clinical research experience to deliver exquisite science, develop valuable insights, and author flawless documentation.
We do it all with a commitment to exceptional service. We’ll 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 better – PRO – your Partner Research Organization.
Preclinical Testing
iuvo offers complete product lifecycle testing - from early stage research to biocompatibility, stability testing, aging studies, and sterilization validation right through product release testing. iuvo's experience helps get your product to the market.
Areas of Expertise:
Clinical Research
iuvo's network of investigative sites is extensive and includes investigators and key opinion leaders, especially in the area of ophthalmology, who have conducted clinical trials for decades. Our network can deliver high-quality, compliant, and timely clinical trials across a wide-array of ophthalmic disease states.
Areas of Expertise:
Consulting Services
iuvo can help you design and execute evidence-based, regulatory-accepted strategies, and guide you through every phase of your product development process – from research to release. Or we can support specific phases of your product development and regulatory journey.
iuvo in action
Case Study - Adaptability
Customer's needs change over time, and over the course of a project. Our offerings can adapt to help respond rapidly to a changing landscape, scaling up and down as needed.
Read MoreCase Study - Development
Some new devices have such a novel approach that there is no defined path to demonstrate safety and efficacy. The iuvo team can work along with our customers to develop new test methods to meet the needs of novel treatments.
Read MoreCase Study - Clinical Research
Time to market is critical for all organizations. Our speed and flexibility enable us to rally to meet difficult challenges, including recruiting critical patient groups in weeks instead of months to meet a tight sponsor deadline.
Read MoreWhat Our Clients Have to Say About iuvo
"We came to the team at iuvo 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
"iuvo has been our partner for sterilization and packaging validation services for the last 8+ years. Their technical strength and customer service focus over the years have really helped iiMED enhance our capabilities as a contract manufacturer of consumable medical devices."
Gregory Gotthelf / Vice President, iiMED
"I have been receiving positive feedback on iuvo’s sterilization requalification reports from our certified body and several of our medical customers. I typically present the data/results from iuvo’s reports during customer audits and it has been stated several times that the reports are well written and the details/data are prepared very well. Keep up the good work!"
Brian Andrich / Manufacturing Engineering Manager, Lumitex, Inc.
"iuvo has been very helpful to my clients. They have found iuvo more responsive, professional, and less costly than other labs in the business. My clients are happy with the recommendation."
Robert Poggie / President, BioVera
"I have found Iuvo to be knowledgeable in helping customers select the correct biocompatibility testing, The reports issued are clear and concise, will withstand regulatory scrutiny, and are submission ready."
Sharon Morford / A Wright Path®
