BioSRL’s scientific and regulatory affairs department assures the goals of a clinical study meets regulatory guidelines. Clinical trial applications (CTA) can also be developed to meet legislative requirements and the team can attend ethic committee meetings to help convey that information to speed approval.
The company’s project management team has extensive experience in coordinating clinical trials across a wide range of therapeutic areas, and utilizing numerous different study designs. The project managers are responsive and provide clients with immediate, long-term support.
In addition, BioSRL’s project managers work closely with external contractors and sponsors to ensure timely communication.