Monitoring and Reporting Adverse Drug Reactions
Who Should Attend
This course is designed for those responsible for the development, communication and facilitation of a product's safety profile within the Pharmaceutical, Biotechnology and Medical Device industries. Personnel who have some experience with adverse event reporting should attend this course; specifically, the following professionals would most benefit from the course:- Drug Safety Associates/Specialists
- Safety Surveillance Professionals
- Clinical/Medical Affairs Directors
- Clinical Research Associates/Managers
- Clinical Safety Specialists
- Project Managers
- Complaint Management Professionals
- QC and Clinical Scientists
- Regulatory Affairs Professionals
- Adverse Event Information Specialists
- Pharmacovigilance Professionals
Booking Options
This course is available exclusively as an onsite training solution. To discuss a solution that fits your organization's needs, objectives, schedule and budget, contact a PTi Client Solutions Manager at 800-303-8194 or OnSiteSolutions@pti-international.com.