- TypeWebinar
- Location Denver, Colorado, United States
- Date 17-08-2018
Business Development
Advertising/Marketing
Manufacturing
Export/Import
Consumer Products
OVERVIEW
This webinar will review the current regulations, guidance documents for GMP Documentation in detail. Regulatory strategies and logistical considerations for early development stage product, including vendor selection and management, stability, labelling, and documentation requirements will also be reviewed and explored.
WHY SHOULD YOU ATTEND
Attend this webinar so that you may understand differences between GMP requirements for early and later stage clinical development. Explore and discuss ways to develop and implement strategies for your GMP documentation.
AREAS COVERED
LEARNING OBJECTIVES
Learn the rules and regulations governing GMP Documentation. Also learn about the development and implementation of strategies for GMP documentation.
WHO WILL BENEFIT
For more detail please click on this below link:
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882
Understand how to develop and implement strategies for GMP documentation and what are the laws and regulations surrounding it.
26468 E Walker Dr, Aurora, Colorado 80016
888300849426468 E Walker Dr, Aurora, Colorado 80016
8883008494 Fax No: Aurora