The European Information Center on Clinical Research Participation (EICCRP) is the first European not-for-profit organisation dedicated to informing and educating patients and professionals on clinical research participation. We aim to improve the public perception of clinical research and the pharmaceutical industry.
Join us on our upcoming workshops and masterclasses focusing on clinical trial audits and inspections, pharmacovigilance, pharma project management and on the EU Clinical Trial Directive regulatory requirements.
Meet and network with business and academic professionals so you can receive latest key information on the market in order to:
- Understand the significance of the increased emphasis on sponsor responsibility
- Learn about the regulatory framework that guides EMA and FDA inspections
- Examine the implications of audit and inspection results
- Expand your safety knowledge
- Ensure you build and maintain a quality Pharmacovigilance Department
- Increase your understanding of project management tools and techniques
- Learn to apply the project management processes to your everyday practices
- Discuss the Clinical Trial Directive process for overcoming its challenges
- Gain an overview of the EU Clinical Trial Directive and GCP Directive
- Ensure you comply with Pharmacovigilance & Adverse Event Reporting
- Discuss clinical trial data management including EDC and e-source
- Understand FDA requirements including recent developments
