| |
|
|
| |
|
|
| |
HUM-MOLGEN
-> Events
-> Courses and Workshops |
|
|
| |
| |
| |
January 17, 2019 |
|
|
| |
|
|
| |
|
|
|
CfPA-The Center for Professional Advancement, New Brunswick, NJ
June 26-27, 2019
Who Should Attend?
This course is designed for those who already have some experience in managing GLP studies; those who wish to extend their role to study direction and their competence in study management, particularly in the complex multi-site environment. The course will benefit the following individuals:
• Existing Study Directors who wish to upgrade their competence in a
multi-site situation
• The newly appointed Study Director
• Study Supervisors who wish to become Study Directors
• Study Monitors
• Principal Investigators in the field of Preclinical Regulatory R&D
• Coordinators of multi-site projects Course Description
|
|
|
|
|
|
|
|
Organized by:
|
|
CfPA-The Center for Professional Advancement |
|
|
Invited Speakers:
|
|
| Philip Withers, GLP training and compliance consultant |
Philip Withers was Director of Quality Assurance at MDS Pharma Services in France and has been involved in preclinical QA for over 35 years. For 25 years he worked in non-clinical contract laboratories in England and France where he set up the quality assurance programme worldwide. Mr. Withers is a member of the organising committee of SoFAQ (the French national QA society), past chairman of the multi-site working party and senior editor of the Quality Assurance Journal. He has presented many papers at international QA meetings and has been involved for several years in developing a variety of training programmes nationally and internationally including OECD training workshops.
Fourteen years ago he created his own GLP training and compliance consultancy.
|
|
|
|
|
|
|
|
Deadline for Abstracts:
|
|
n/a
|
|
|
|
|
|
|
|
Registration:
|
|
Please click here for registration information.
|
|
|
E-mail:
|
|
Jmorbit@cfpa.com
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
|
|
|
|
|
|
|
|
|
|
|
|
Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp,
Frank S.
Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved.
Liability, Copyright and Imprint. |
|
Dealing with the increased range of duties and responsibilities of study managers is the core issue of this course.
The course goes further than presenting the theoretical roles of study managers in the difficult arena of multi-site studies. The workshop based activities address the practical aspects of study direction and investigate possible solutions to ensure full compliance.
A strong feature of this course is the high level of interactive, dynamic problem solving situations that the participants are asked to resolve appropriately and speedily. The strategies available for managing compliant studies are given topmost priority.
The presenter recognizes that many courses can provide information, but information can only be turned into knowledge through the depth of understanding that comes from sharing experience and exchanging ideas. This is why a workshop approach is so valuable.
Maximize Your Learning!
Attend this course and its Companion Courses:
Good Laboratory Practices (GLP)
June 19-21, 2019 • New Brunswick, NJ • Course ID #545
GLP and Quality Assurance: Developing a GLP Compliant QA Program
June 24-25, 2019 • New Brunswick, NJ • Course ID #2564