THE EFFECTIVE CRA /
CLINICAL TRIAL
ADMINISTRATOR /
COORDINATOR

THE EFFECTIVE CRA / CLINICAL TRIAL ADMINISTRATOR / COORDINATOR

THE EFFECTIVE CRA /
CLINICAL TRIAL
ADMINISTRATOR /
COORDINATOR

How you can be more Proactive in your Role

How you can be more Proactive in your Role

Conference Date: 27-28 Jan 2011
Conference Ref: A1-4211
Fee: £1125 + VAT
Venue: The Rembrandt Hotel, London

This interactive course will provide you with the skills and knowledge to be a successful and effective CRA or member of Clinical Trial Support staff. It covers all the key aspects which CRAs and support staff are likely to be involved in as well as the most important interpersonal skills necessary to be an effective CRA

This will include:

Planning and preparation for setting up clinical trials
Understanding the responsibilities at both the study site and the sponsor site
How to carry out the crucial study site visits including
How to prepare for an audit and/or regulatory inspection
Technological advances on collecting data - EDC
On finishing the course you will then be up to date on the latest regulatory GCP requirements including the EU Clinical Trial Directive and Implementation texts, and the GCP Directive.

Click here to book your place on this important Annual Event

20 * PERIODIC SAFETY UPDATE REPORTS (PSURs)
* CONTRACT LAW 2012

21 * PHARMACOVIGILANCE ASPECTS OF LICENSING AGREEMENTS

22 * DEVELOPING MEDICINES FOR COMPANION ANIMALS

24 * AVOIDING PITFALLS IN PATENT KNOW HOW LICENCES AND R&D COLLABORATIONS

27 * REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 1
* DEALING WITH DIFFICULT PEOPLE

28 * EFFECTIVE PERFORMANCE MANAGEMENT
* REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 2
* PHARMACEUTICAL REGULATORY AFFAIRS IN: RUSSIA, BELARUS & UKRAINE

29 * INTRODUCTION TO POST MARKETING SURVEILLANCE AND MEDICAL DEVICE VIGILANCE SYSTEM