Episode 3: Pharmacovigilance & Adverse Reactions
In our final part of this three-part series on Regulatory Affairs in complementary medicine, we welcome back Sue Woldt, Senior Regulatory Affair Manager at Integria Healthcare.
In part three of this series, Sue will cover adverse reactions and pharmacovigilance and your responsibilities as a practitioner.
Sue discusses
- Definition of Pharmacovigilance (PV)
- What is the difference between an adverse reaction and adverse event
- Who is responsible for reporting adverse reactions and events
- Reporting an adverse reaction
- Wider implications- labelling and warnings
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