Benefits of attending
- Gain a clear understanding of global and local literature searching and regulatory requirements
- Learn how assessments help refine literature evaluation and reporting abilities
- Explore how to assess safety data to identify potential risks and compliance needs
- Develop critical analysis skills for interpreting safety data from literature
- Discover how to effectively manage literature searches within pharmacovigilance processes
Certifications:
- CPD: 12 hours for your records
- Certificate of completion
Course Content
Day 1
Course Provider
Mr Graeme Ladds,
Director ,
PharSafer Associates Ltd.Graeme Ladds, Director of PharSafer, has over 30 years’ experience working in the pharmaceutical industry. Having started his career at Ashbourne Pharmaceuticals in 1989 as Head of Drug Safety & Medical Information, he went on to become Head of Global Pharmacovigilance at Shire Pharmaceuticals. He then set up his consultancy and specialist CRO company, PharSafer Associates Ltd, where he has been involved in establishing pharmacovigilance in companies, performing audits across Europe and the USA, SOP writing, acting as QP for companies, and helping with regulatory inspections.
Who Should Attend
Professionals working within these industries, who want a comprehensive introduction, will benefit from this engaging course:
- Clinical
- Pharmacovigilance
- Regulatory
