The bad news is we cancelled our webinar on the revised Common Rule. The good news? We cancelled it because it seems the revised Common Rule implementation and transition have actually been relatively smooth.
Many of the revised Common Rule’s changes aim to make informed consent more meaningful, so that research subjects have the
Most requirements of the revised Common Rule go into effect January 21, 2019*. While many US researchers are aware of
Gene therapy research has moved from the realm of science fiction to mainstream clinical research. The maturation of this field
The Advarra team is proud to announce that all major integration activities are now complete. SOPs have been harmonized; staff
When research is being conducted in multiple countries, determining which regulations apply to which country’s sites can sometimes be complicated.
The right to try movement and recent passage of the federal right to try law have renewed public interest in
The European Union’s General Data Protection Regulation (GDPR) goes into effect May 25, 2018, replacing the existing EU Data Protection
The Advarra team has worked to fully integrate our processes and policies to provide clients with unified capabilities and support
The Advarra team (formerly Chesapeake IRB and Schulman IRB) continues to integrate our processes and policies, leveraging mutual strengths in
Clinical research continues to grow throughout the world, with researchers looking outside the US for new and diverse subject populations to help develop and improve investigational therapies.
New to clinical research? Learn the meaning of common industry acronyms and abbreviations including eCRF, IIT, PI, TMF, and more.
