2017 - Packaging and Labelling for Clinical Products

Overview:
The program will review how to establish an effective artwork change management and approval system, including real-life examples of system successes and potential pitfalls.
Why should you Attend:
Program will discuss practical development of packaging design and optimizing the design to fit the intended purpose. You will learn to translate a protocol into optimal package design. A review of the compliance requirements between commercial and clinical packaging and labeling will be completed. Review a case study of changing commercial packaging for optimization.
Areas Covered in the Session:
Commercial packaging compliance
Commercial labeling compliance
Clinical packaging compliance
Clinical labeling compliance
Change control for materials, design and content)
Pharmaceutical (drug/biologic)
Who Will Benefit:
Manufacturing personnel
Quality and compliance personnel
Regulatory personnel
Clinical operations
Speaker Profile:
Peggy J. Berry , MBA, RAC, is the President & CEO at Synergy Consulting where she provides consulting services to companies in all aspects of drug development. She also provides group and one-on-one training in drug development, regulatory affairs and project management topics. Prior to founding Synergy Consulting in 2015, she was Vice President of Regulatory Affairs at Insmed (2/2015-5/2015) where she was responsible for the development and implementation of global regulatory strategies and the management and oversight of the regulatory affairs department.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com