Goodwyn IRB provides a wide range of services for the review and oversight of clinical research. Our customers are pharmaceutical and device manufacturers (sponsors) and the contract research and site management organizations that serve them. We also serve institution and physician-sponsors.

Here's our list of services. Or, perhaps we can design a custom program to fit your unique requirements.

Initial and ongoing review of clinical research protocols and investigative sites (including the informed consent process and study-related materials).

On-line IRB submission tracking

Delivery of IRB review documentation within 48-hours of the review

Good Clinical Practice (GCP) audits and training.

On-site evaluation of the informed consent process.

Informed consent writing, templates & translations.

Statistical support for de-identification of protected health information

Call us at 877-793-8900 to discuss your needs.

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