BETHESDA, Md., Sept. 25, 2019 /PRNewswire-PRWeb/ -- The Parenteral Drug Association (PDA) today announced the availability
Martin Van Trieste, Civica President & CEO, a former Amgen executive and PDA Immediate-Past-Chair, and Susan Schniepp, industry consultant and former PDA Director, co-chair the purchasing controls committee.
"Historically in our industry the people who make the decisions on which suppliers to select in the negotiations of the contract are not in the quality unit or even manufacturing; they are in procurement or sourcing or a purchasing organization," Van Trieste said. "We feel it is important not only does everyone have to be involved in the quality of the product, that the people who actually make those decisions are held accountable and this new ANSI standard will help do that."
PDA is advancing five other standards
More information about PDA's role in standards development: https://www.pda.org/scientific-and-regulatory-affairs/pda-ansi.
Find answers to standard development questions: https://www.pda.org/scientific-and-regulatory-affairs/pda-standards-frequently-asked-questions or reach out to email@example.com.
About PDA – Connecting People, Science and Regulation® The Parenteral Drug Association (PDA) is the leading global provider of science, technology and regulatory information and education for the pharmaceutical and biopharmaceutical community. Founded in 1946 as a nonprofit organization, PDA is committed to developing scientifically sound, practical technical information and resources to advance science and regulation through the expertise of over 10,500 members worldwide. Go to http://www.pda.org/footer/about-pda to learn more.
SOURCE PDA, Inc.