The European Pharmacovigilance & Clinical Trials 2016 offers a one of a kind discussion platform for pharmaceutical experts to debate and discuss the challenges they are facing in Pharmacovigilance and Clinical Trials.
Do not miss out on the chance to acquire first-hand knowledge and experiences from pharmaceutical giants such as AstraZeneca, Merck Sereno, Boehringer Ingelheim, Pfizer, Novo Nordisk, Johnson & Johnson, Novartis and many more on the latest technological advances in data capture and effective feasibility models. We will be addressing topics such as major challenges faced by EU legislation and emerging economies and PV harmonization, adverse event reporting and PV & clinical trials, clinical trials signal detection and many others. Join us and be future ready!
Take advantage to meet the leading experts within the field and discuss the latest challenges all your competitors are facing.
We are looking forward to welcoming you on board in 2016!
KEY HIGHLIGHTS:
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鈥� 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鈥�
Conference Booking Details:
Delegate Fee & Discounts:-
Early Bird Registration Fee - 拢 699 + VATfrom 29 July- 30 Aug 2016
Standard Registration Fee - 拢950 + VAT from 31 Aug- 24 Oct 2016
Introductory Offer - 3 delegate places for the price of 2 - (Limited seats left)
Maximise Your Involvement through sponsorship and exhibition opportunities Our sponsors are an integral part of the CGE Conference and we want to ensure you receive the best possible results for your investment. Exhibiting and sponsorship options are extensive, and packages can be tailor-made to suit your individual company's needs.
Do not miss out on the chance to acquire first-hand knowledge and experiences from pharmaceutical giants such as AstraZeneca, Merck Sereno, Boehringer Ingelheim, Pfizer, Novo Nordisk, Johnson & Johnson, Novartis and many more on the latest technological advances in data capture and effective feasibility models. We will be addressing topics such as major challenges faced by EU legislation and emerging economies and PV harmonization, adverse event reporting and PV & clinical trials, clinical trials signal detection and many others. Join us and be future ready!
Take advantage to meet the leading experts within the field and discuss the latest challenges all your competitors are facing.
We are looking forward to welcoming you on board in 2016!
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鈥� 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鈥�
Conference Booking Details:
Delegate Fee & Discounts:-
Early Bird Registration Fee - 拢 699 + VATfrom 29 July- 30 Aug 2016
Standard Registration Fee - 拢950 + VAT from 31 Aug- 24 Oct 2016
Introductory Offer - 3 delegate places for the price of 2 - (Limited seats left)
Maximise Your Involvement through sponsorship and exhibition opportunities Our sponsors are an integral part of the CGE Conference and we want to ensure you receive the best possible results for your investment. Exhibiting and sponsorship options are extensive, and packages can be tailor-made to suit your individual company's needs.
