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This life science product stability testing webinar will explain, in detail, the requirements of the FDA’s drug stability guidelines that are stipulated for drug products and how to design a product stability testing plan that can be applied to new or modified products in the pharmaceutical, biotechnology and medical device industries.
Why Should You Attend:
To avoid mistakes and misinterpretations while designing a new drug stability testing program or while modifying existing ones, it’s best to have a clear knowledge of the regulations and guidelines stipulated by the FDA, 21 CFR and other regulatory bodies.
Who Will Benefit:
The webinar will benefit people within the pharmaceutical, biotechnology or medical device industries that currently have a stability testing program but are not savvy about maximizing the use of their data for extending their product’s expiration dating. The employees who will benefit most include:
Quality Control Analyst and Management
Senior Management
Manufacturing Associates and Management
Shipping and Distribution Personnel
Stability Testing Department Personnel and Management
Instructor Profile:
Charity Ogunsanya, is the CEO and founder of Pharmabiodevice Consulting LLC. Ms. Ogunsanya has over 23 years of extensive practical and management experience in various Fortune 100 pharmaceutical, biotechnology, biologics, cell therapy, diagnostics, research and development, radio-pharmaceutical, Contract Manufacturing Organization (CMO) and medical device/IVD companies.
Note:
Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.
For Registration:
http://www.complianceonline.com/new-drug-device-stability-testing-program-fda-guidelines-webinar-training-703000-prdw?channel=eventsinamerica
Source : Event Website
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