Clinical Trials

San Francisco Research Institute understands your need to move your product through the development pipeline expediently.  The Phase I – IV clinical trials done at our institute are completed in a timely manner. We work closely with sponsors and CROs to insure the best quality of clinical research.  

Safety & Efficacy

Together with our time we provide vast testing services surrounding clinical safety, efficacy (claims substantiation) and research. Testing methodologies include, but are not limited to:

  • Clinical safety – regulated and safe to use product formulas and devices.

  • Clinical efficacy – ensuring that products do what they are designed to do.

  • Clinical research – comparative evaluations, guarantee that a product holds up against competitors or other versions of your formula. 

All of these services are provided to sponsors and CROs that partner with SFRI.

Testing Capabilities

We offer a full spectrum of regulatory, scientific, and testing solutions. We have the the expertise and in-house capabilities to perform all requirements for clinical trials. 

  • Standard Clinical Research and Testing

    • Routine type of studies that are Sponsor supported

    • Pharma (OTC and Rx) Studies

    • Dermatology Studies

    • Pharmacokinetics and Bioavailability Studies –Dermal, Oral and IV

    • Bridging Studies

    • Cosmetic –Claims Substantiation & Safety

    • Dietary Supplements

    • Cannabinoids

  • Innovative & Advanced Studies

    • Mechanistic studies

    • Advanced Measurements

    • Studies using Advanced Technology & Skin Imaging

    • Advanced Technology

Multi Speciality

  • Internal Medicine 

  • Gastroenterology 

  • Obstetrics and Gynecology 

  • Infectious Disease 

  • Cardiology 

  • Ophthalmology 

  • Dermatology 

  • Women’s and Men’s Health

  • Endocrinology: Diabetes & Obesity

  • Hair Treatment & Restoration

  • Pain Management

Management & Consulting

In addition to being a clinical research site we also offer management and monitoring capabilities along with consulting.

  • Clinical Research & Scientific Product Development

  • International Regulatory Compliance & Management

  • Medical Affairs Services

  • Product, process and clinical operations development from concept to commercialization of pharma, medical devices, diabetes devices, wearables) dermatology, beauty, and personal care, dietary supplements,, functional foods, and cannabinoid, clinical testing, regulatory compliance and project management,

  • Design, and substantiate long lasting, and ownable claims,

  • Design and manage development of products for multi ethnic patients and consumers (pharma. devices, skin care, dermatology, and dietary supplements)

  • Develop testing methodologies and claims substantiation methods for health and consumer products for multi ethnic population

  • Recruit Global panels of multiethnic patients and subjects to participate in clinical trials of pharm, consumer products globally

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