PVPlan software enables users to create and manage a Pharmacovigilance Plan, in accordance with the EU Risk Management Plan Template (EU-RMP). With PVPlan, product safety professionals can document identified and potential safety concerns for a product, and track actions, accountable persons, status, and related milestones for characterizing those concerns and identifying additional concerns. The web-based platform allows diverse and geographically separated teams to collaborate and share information through the product lifecycle, and to manage pharmacovigilance. PVPlan helps clients document all safety concerns for a product, not just signals generated after a product launch or through data mining.
PVPlan Benefits:
- Document Safety Concerns and associated actions throughout the product lifecycle, with an easy-to-use, web-based platform.
- Develop and maintain a Pharmacovigilance Plan consistent with EMEA Risk Management Plan (EU-RMP) template.
- Share information and manage pharmacovigilance actions among diverse and/or geographically distributed teams.
- Option to integrate the results of quantitative signal detection into the documentation process
