Packaging and Labelling for Clinical Products

Packaging and Labelling for Commercial and Clinical Products


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@compliance4All.com

Ad Reference ID: 28758abdef122533

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