Скачать или смотреть Integrating Quality Culture in Life Sciences and Medtech

Ensuring quality across manufacturing operations remains a major concerns for many quality and compliance managers within organizations. Some steps were taken by the FDA Quality Metrics initiative to assist companies in tackling issues. But was it enough?

Learn about some of the best practices to build quality cultures in this Redica Systems recorded Webinar: “Past, Present, and Future of Quality Culture”
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Learn more about Redica Systems and what it can do for your company: https://redica.com/request-a-demo/

What will you learn?
-How the 2014 FDA Quality metrics initiative led to a greater focus on quality culture
-New quality culture tools and standards under development by PDA and other organizations
-Best practices for quality culture, including case studies with lessons learned

About the expert
Susan Schniepp, Distinguished Fellow at Regulatory Compliance Associates, ® Inc., is the knowledge leader responsible for training and advising RCA staff and clients on current trends and issues facing the pharmaceutical, biotechnology, and medical device industries. Her background includes cGMPs, audit readiness, change control, investigations, supplier quality, and batch record reviews.

She has more than 40 years of experience in quality assurance, serving in leadership roles at Allergy Laboratories, Inc.; OsoBioPharmaceuticals LLC; Searle; Abbott; and Hospira. In addition, she has been on the Parenteral Drug Association (PDA) Board of Directors from 2011-2013 and 2016-2019 and currently serves as the Chair-Elect.

Learn more about Redica Systems and what it can do for your company: https://redica.com/request-a-demo/