Pharmacovigilance is responsible for the collection, assessment, identification, and communication of all drug safety information. In addition, PV focuses on the processing of safety information, adverse event reporting, and keeping up to date with guidelines and regulations.
The 2nd Pharmacovigilance Oversight and Inspection Readiness Summit will focus on how to achieve safety inspection readiness through effective partner collaboration and quality optimization strategies.
Sponsorship is a great way to enhance your brand’s visibility and help you connect with top-level decision-makers, innovators, and industry disruptors. There are a number of ways to maximize branding opportunities at the summit.
To learn about sponsorship opportunities, please contact Meg Larson at Meg@momentumevents.com
Top Reasons to Attend
Analyze the importance of a Culture of Quality and its impact on safety
Prioritize patient support programs
WHO SHOULD ATTEND
- Safety & Risk management
- Drug safety
- PV Compliance
- Safety Surveillance
- Medical Affairs
- Regulatory Affairs
- Inspection and Audit
- Post-market studies
- Medical product safety assessment
- Drug Research & Development
- Clinical Pharmacology
- Medical information
- Health outcomes