CRO Preclinical & Clinical Laboratory Services

Marin Biologic Laboratories has been developing, validating and testing PK and clinical samples under GLP/GMP compliance for the last 10 years. The company has recently moved into its state of the art facility to further aid our clients with these projects. To further our client services, we pride ourselves on unparalleled communication.

Typically, our clients will have a confidentiality agreement with Marin Biologic and a master services agreement if samples are involved. When you call, or email us, a Ph.D. experienced in the areas of IND or NDE or other FDA regulated drug applications or communications will assist you in developing your custom project.

If you have identified your goals, strategies and methods our staff will develop a proposal using your specific requirements. If you are unsure of your strategy, a Ph.D., scientist will assist you to discuss the pros and cons of different approaches

A cost and time estimate will be communicated as the proposal is being developed, so the if there are changes based on these factors, they can be captured at the early stages. We try to present strategies that will save you costs and time, like bundling samples together.

Once completed, the proposal is transmitted to you for review, whereupon if further changes are required they will be inserted into the proposal. During the development of your proposal the start date will be discussed and the transfer of reagents, drugs or samples.

> Bioanalytical Assay Development
> Assay Validation
> Preclinical & Clinical Testing Services
> Cell Based Assays (Potency)
> Immunoassays (Cell Based & ELISA)
> Biochemistry Assays
> Stem Cell Assays
> Regulatory
> In Vitro Toxicity