How Can We Help You?
How can I get a quote for a preclinical trial or study?
To receive a quote for your preclinical trial or study, please contact a member of our sales team:
After a Non-Disclosure Agreement (NDA) is in place, your Surpass contact will request a description of proposed research, and will set up a meeting with members of the Surpass Research team as necessary for further discussion and questions. Following this discussion, a detailed proposal, including a quote, will be provided to you.
How long does it take to start a preclinical trial or study once the quote is approved?
An Institutional Animal Care and Use Committee (IACUC) document must be completed and approved for any work involving live animals. Surpass can schedule your project as quickly as resources allow, and will work with you to put the appropriate IACUC documentation in place. We understand how scheduling can impact project timelines, so will work with you to complete your high quality research as efficiently as possible.
How long does it take for an IACUC document to get approved?
To ensure appropriate time for review by our committee, we ask that IACUC documents be submitted two weeks in advance of a study. Our scientists will assist you in answering any questions around this process. Please contact Surpass to discuss accelerated project needs.
How do I schedule a quality audit?
To schedule a quality audit, please notify your sales contact or call the head of quality assurance:
Can I bring my own surgeon or interventionalist to perform the experimental surgery in the study?
Surpass welcomes our sponsors’ physician advisors to participate in studies. Written qualifications and/or a CV must be provided to the Surpass IACUC in advance of the project for approval.
Can our engineers or clinical staff participate in the study?
Surpass welcomes individuals with appropriate training and experience to participate in studies. Written qualifications and/or a CV must be provided to the Surpass IACUC in advance of the project for approval.
Does Surpass perform GLP preclinical studies?
Surpass has years of experience conducting GLP preclinical studies for regulatory submissions and IRB approval, and provides qualified study directors and on-site veteran quality assurance auditing to ensure the success of your study. See GLP Services for more information.
Do you have additional questions?
Contact our sales team: