| |
|
|
| |
|
|
| |
HUM-MOLGEN
-> Events
-> Courses and Workshops |
|
|
| |
| |
| |
April 17, 2019 |
|
|
| |
|
|
| |
|
|
|
CfPA-The Center for Professional Advancement, Online Live
June 25, 2019 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend?
The introductory training will provide an overview of the key procedures and techniques involved in the preparation of clinical trial supplies. The training is intended for those who are new to clinical supplies or individuals who may interact with clinical supplies personnel /third party providers and want to understand the clinical supply chain or re-fresh their knowledge.
This online training will benefit professionals in the following industries:
• Pharmaceutical
• Biotechnology
• Contract Clinical Research (CRO)
• Contract Clinical Packaging and Logistics
Thus, it will be of interest to those in the following Job Functions:
• Packaging
• Clinical Manufacturing
• Clinical Trial Label Design
• Clinical Research Associate
• Logistics
• Quality Assurance/Quality Control
• Interactive Voice Response Systems- IVR/IWRS
• Hospital Pharmacists Involved in Clinical Trials
In Departments such as:
• Research and Development
• Quality
• Clinical Supplies
• Clinical Course Description
|
|
|
|
|
|
|
|
Organized by:
|
|
CfPA-The Center for Professional Advancement |
|
|
Invited Speakers:
|
|
 Esther Sadler-Williams, Managing Director, SimplyESW |
Ms. Sadler-Williams is currently Managing Director, of her own Clinical Supply training and consultancy company – SimplyESW, an organisation that supports clients in enhancing team skills as well as conducting improvement projects to optimise clinical supply chain delivery.
Prior to this, Ms. Sadler-Williams was Senior Director of Strategic Alliance Development and Innovation for Catalent Pharma Solutions. Catalent acquired Aptuit CTS in February 2012, a company which had previously acquired Almedica where Ms. Sadler-Williams was a founder member of the European facility. Almedica provided contract services for clinical supplies including packaging, labelling and distribution.
|
|
|
|
|
|
|
|
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. |
|
Examples will be provided of strategies that can be employed to ensure the overall supply chain can work flexibly with changes in clinical trial design.
Can't Make this LIVE Webinar?
Simply select the On Demand option when registering and we will send you the link to view the recorded version.
On Demand available approximately 3 business days after the live offering.