This web seminar will deliver an introduction to the basics of drug safety and pharmacovigilance, including regulatory requirements, Adverse Event reporting, signaling, and risk management. Successful navigation of drug safety and pharmacovigilance are keys to product longevity, consumer confidence, and regulatory compliance. This web seminar will also provide learners with the regulatory references, processes, best practices, and analysis and investigation techniques to minimize risk, avoid product recall, and meet international safety and reporting standards.
- Work to international standards by meeting regulatory requirements for product safety
- Collect, assess, report, and analyze Adverse Events
- Identify differences between U.S. and European legal requirements
- Clinical Safety/Pharmacovigilance Specialists
- Regulatory Affairs Professionals
- Quality Management Specialists
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Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will mail ACPE statements within three weeks of program completion. ACPE#: 0778-0000-11-027-L01-P. Released: 2/11.
Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.