We have a dedicated and experienced team focusing on clinical trial applications to the regulatory and ethics committees. We have submitted clinical trial applications across many regions for a range of products which includes simple molecules, advanced therapies and biologics.
Our aim is to lead and advise you to achieve a positive clinical trial authorisation. We advise every step of the way and communicate closely with you and the regulator to achieve a positive outcome.
Below is a list of our services related to clinical trials:
– Submission and management of clinical trial applications in global markets
– Ethics committee submissions for clinical trial’s in global markets
– Monitoring and site management
– Clinical trial document management
– Statistical analysis support