Pharmacovigilance and clinical trials have evolved considerably in the past few decades to meet the expectations of the public and modernization of human health. With the ever-increasing globalization, communication, Internet access, free trade across countries and easy access to drugs there is continuing demand for further development and stringencies in PV and clinical trials.
European Pharmacovigilance and clinical trials conference 2016 will provide an opportunity to all its attendees to discuss, share and stay updated with present state of affairs in Pharmacovigilance and clinical trials. It will also allow all its participants to discuss the various developments, challenges faced and innovations in the field. The conference will attempt to explore the reforms required to enhance drug safety and public health. The conference will also provide all its participants an opportunity to network with various pharmaceutical industries; clinical research organizations and PV service providers.
It gives us a great pleasure welcoming you to the European Pharmacovigilance and Clinical Trials 2016 conference.
KEY HIGHLIGHTS
- Harmonization and Pharmacovigilance
- PV regulations and challenges
- The new EU legislation on clinical trials, its impact and future
- Risk management and minimization
- Adverse drug reactions reporting
- Signal detection and post authorization safety
- Business development and models in clinical trials
- Clinical data management
- Good Clinical Practices and Good Pharmacovigilance practices
- IT and new technologies for improvement of PV and clinical research
- Strategies to improve clinical trials and PV
- Implications of BREXIT
WHO SHOULD ATTEND THE CONFERENCE
CEO’s, CTO’s, CIO’s, Presidents, Vice Presidents, Directors, Heads & Managers, Scientific Advisors, Consultants and professionals from pharmaceutical and biotechnology industries, CROs and service providers involved in Pharmacovigilance or Clinical Trials. Attendees’ job responsibilities include:
- Pharmacovigilance
- Safety & Risk management
- Drug safety
- QPPV
- PV Compliance
- PSMF
- Safety Surveillance
- Medical Affairs
- Signal detection
- Regulatory Affairs
- Inspection and Audit
- Pharmacoepidemiology
- Clinical Operations
- Clinical Research and Development
- Clinical Quality Assurance/Control
- Clinical Compliance
- GCP
- Clinical Monitoring
- Clinical Data Management
- Contract outsourcing service providers
- IT consultants
SPEAKERS
There are plenty of opportunities to position yourself as a thought leader & showcase your company.
For enquiries on speaker opportunities please e-mail to speaker@corvusglobalevents.com
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