RMP Development and Maintenance

The Risk Management Plan (RMP) is the scientific document that intends to bring everything together concerning your product safety profile. This pivotal document maintains the overview of all risk, efficacy, and safety data.

With our in-house regulatory, clinical development, and quality teams’ support at their disposal, our pharmacovigilance (PV) specialists manage the development of a high-quality RMP that meets all regulatory requirements and ensures its periodic updates.

Shortly, we help you set up your RMP to identify and distinguish drug product’s risks concisely and efficiently, leaving you with additional time to spend on your drug development or commercialization.