Custom Solutions Tailored to Your Unique Product
At Accorto, we manage our client’s regulatory compliance needs at every stage of the product approval process. This includes offering a wide range of clinical and non-clinical studies designed to generate the essential data needed for your application to properly demonstrate the safety and efficacy of your products.
To fulfill our client’s unique data requirements, we combine our in-house regulatory, leadership, and technical teams with an extensive network of top-tier global CROs and industry experts, seamlessly integrating our services with our trusted CRO partners to address your unique regulatory challenges swiftly and effectively.
Clinical Studies
- Protocol Design & Development
- Protocol IRB Approval
- Clinical Trial Oversight & Management
- Performance Testing
- Product Usability & Label Comprehension Testing
- Consumer Research Studies
- Longitudinal Cohort Studies
Non-Clinical Studies
- Biocompatibility
- Toxicology
- Microbiology
- Virology
- Bacteriology
- Bio Analytical
- Chemical Testing
- Stability Testing
- Product Composition & Label Accuracy
- Organic & Inorganic
- Packaging Extractability & Leachability
The Right Resources.
The Right Time.
When you choose Accorto, you gain access to our global network of CRO’s, hand-selected for their specialized knowledge, state-of-the-art facilities, and track record of delivering exceptional results.
Our network is constantly expanding, allowing us to keep pace with industry advancements and deliver cutting-edge solutions for our client’s unique projects.
Contact Us Today
to discuss how Accorto can develop bespoke clinical and non-clinical studies to support your regulatory applications.
