THIS TRAINING ON PHARMACEUTICAL STABILITY STUDIES 2015 - Stability Program to Support Shipping and Distribution of Drug Products

Website http://bit.ly/1ASq1Wv | Edit Freely

Category FDA GXP Compliance - Pharmaceuticals

Deadline: February 11, 2015 | Date: February 11, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2015-02-10 19:44:58 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

A drug product must maintain its identity, strength, quality and purity till its expiration. Physical, chemical and biological data are influenced by various environmental factors such as temperature, humidity and light. In current manufacturing environment, products can be shipped and distributed across different climatic zones. Seasonal changes as well as types of transportation can greatly affect the supply chain of the products.

Who Will Benefit:

Pharmaceutical scientists

Manufacturers of raw material and ingredients

Analysts and lab managers

QA managers and personnel

Instructor Profile:

Kim Huynh-Ba has almost 25 years of experience in analytical development, project management, strategic drug development and stability sciences. She is the executive director of Pharmalytik, where she provides consulting and training services to pharmaceutical companies including companies operating under FDA’s consent decree on harmonization and optimization of analytical best practices.