Latest Parenteral Drug Association Stories
BETHESDA, Md., March 7, 2013 /PRNewswire-USNewswire/ -- The Parenteral Drug Association (PDA) announced today that three high-level regulators from the United States and Europe will speak at the 2013 PDA/FDA Process Validation Workshop, May 20 - 21 at the Hyatt Regency in Bethesda. They are: Jeffrey Baker, Deputy Director, Office of Biotechnology, CDER, FDA Lina Ertle, Quality Assessor, ANSM (France) Patrick Swann, Deputy Director, Division of Monoclonal Antibodies, CDER, FDA...
BETHESDA, Md., Feb. 26 2013 /PRNewswire-USNewswire/ -- The Parenteral Drug Association (PDA) announced today that Richard Friedman, Associate Director OMPQ, U.S. FDA, and Rebecca Rodriguez, Consumer Safety Officer, U.S. FDA, have been confirmed to deliver the closing plenary talks at the 2013 Human Factors and Human Error Reduction Workshop. The workshop will take place on April 17 - 18, 2013 at the Peabody Hotel in Orlando, Fla. (Logo:...
BETHESDA, Md., Dec. 11, 2012 /PRNewswire-USNewswire/ -- The Parenteral Drug Association is pleased to announce that the new members only PDA Technical Reports is now open. "This is the most innovative and significant member benefit ever offered by The Parenteral Drug Association (PDA)," said Richard M. Johnson, PDA President. "We have been working hard on enhancing our member value and we believe that releasing this new Technical Report Portal by the end of 2012 is a breakthrough...
LIONVILLE, Pa., Oct. 11, 2012 /PRNewswire/ -- West Pharmaceutical Services, Inc. (NYSE: WST), a global leader in innovative system and component solutions for injectable drug administration, today announced that company representatives will be speaking in several educational sessions and showcasing West's innovations at the Parenteral Drug Association's Universe of Pre-filled Syringes & Injection Devices conference in Las Vegas, October 15-17, 2012, booth #303. (Logo:...
BETHESDA, Md., Sept. 24, 2012 /PRNewswire-USNewswire/ -- The Parenteral Drug Association is pleased to announce that by the end of 2012 PDA members will be able to view all PDA Technical Reports through our new Technical Report Portal. "This is the most innovative and significant member benefit ever offered by The Parenteral Drug Association (PDA)," said Richard M. Johnson, PDA President. "We have been working hard on enhancing our member value and we believe that releasing this...
BOSTON, April 11, 2011 /PRNewswire/ -- PAREXEL International Corporation (NASDAQ: PRXL), a leading global biopharmaceutical services provider, and the Parenteral Drug Association (PDA) today announced the publication of Quality by Design: Putting Theory into Practice, written to help companies maximize product quality and safety. As increasing regulatory pressure is being placed on biopharmaceutical companies to be accountable for Quality Systems, the book serves as a definitive source on...
DUBAI, UAE and JOHANNESBURG, February 17, 2011 /PRNewswire/ -- The European Medicines Agency (EMA) has published a concept paper on storage conditions during transport (EMA/INS/GMP/638479/2010). The goal is to create new Good Distribution Practice (GDP) and GMP guidance and may lead to the need to revise the guideline on declaration of storage conditions (CPMP/QWP/609/96/Rev2). Over the past few years, significant changes continued to occur in the globalisation of manufacture with...
