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REGULATORY CONSULTATIONS

Subject Informed Consent Preparation

At Principal, protection of Research Participants is our passion and top priority! With years of experience in Phase I - IV Clinical Trials and as experts in the industry, we understand the complexity and importance of your study’s informed consent. The staff at Principal IRB is fully trained in ethical consent preparation and understands how to properly utilize the four key components that are essential for any informed consent.  

Good Clinical Practice Audits

Principal IRB now offers Good Clinical Practice  (GCPs) customized audits. These audits are specialized to your specific needs and include, but are not limited to:  Investigator Practices, Contract Research Organizations (CROs)  and Regulatory Consultations.

Training

Are you an Investigator new to clinical research? Is your site, sponsor or CRO interested in updating your team on the latest industry gold standards? At Principal IRB we are proud to offer customized Investigator training, CRA training and CRC training. 

If you are interested in informed consent preparation, GCP Audits or training by Principal for your study or staff, please CONTACT US or call 1-386-626-3038. 

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