BioClinAarcteam supports clinical trials and post-marketing safety surveillance. We are working globally.
BioClinAarc is currently performing end to end services Globally, involving all therapeutic areas.
BioClinAarc can provide integrated or stand-alone services to support product safety monitoring in compliance with regulatory requirements for safety surveillance in pre- and post-approval settings.
We Offer this services for all the stages of clinical trial development, risk management and assuring safety during the complete clinical development and post-approval.
Pharmacovigilance includes the following services :
Medical Monitoring
Coding of adverse events and medications (MedDRA and WHO Drug)
Review and management of suspected serious adverse reactions
Preparation of MedWatch and CIOMS forms
Preparation of safety narratives
Individual Case Safety Report (ICSR) processing for serious adverse events
Management of adjudication and data safety monitoring committees
This section of our website will enable you to learn more about becoming an BioClinAarc Investigator and also provides a dedicated resource centre for Investigators working with BioClinAarc Central Laboratories.
