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Parenteral Drug Association
Connecting People, Science and Regulation
®
Parenteral Drug Association
Connecting People, Science and Regulation
®
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Press Releases
10/19/2010
Hear from the FDA, National Institute of Health and More at PDA Freeze Drying Workshop
Hear from the US FDA, National Institute of Health and More at PDA’s 2010 Pharmaceutical Freeze Drying Workshop
10/17/2010
Maik Jornitz, Was Promoted to Head, Operational Marketing of Sartorius Stedim Biotech
PDA’s Board of Director’s Chairman, Maik Jornitz, Was Recently Promoted to Head, Operational Marketing of Sartorius Stedim Biotech.
09/19/2010
Over 800 Regulators and Scientists Attended the 2010 PDA/FDA Joint Regulatory Conference
Bethesda, Md. – PDA/FDA's Joint Regulatory Conference recently held in Washington, D.C. has been an overwhelming success with over 800 regulators and scientists attending and discussing current and upcoming regulatory trends and quality requirements.
09/01/2010
Hear from the US FDA, the Australian Therapeutic Goods Administration, the Japanese at PMDA
Bethesda, Md. – The Parenteral Drug Association (PDA) is proud to announce the confirmation of expert regulatory speakers at this year’s Global Conference on Pharmaceutical Microbiology.
08/30/2010
The FDA to Provide Perspective on Current Training Issues at PDA’s Biennial Training Conf
Bethesda, Md. – The Parenteral Drug Association (PDA) is proud to announce that Rebeca Rodriquez, National Expert Investigator, FDA is confirmed to give an Overview of Personnel Qualification Issues found during FDA Inspections in Baltimore, Maryland on October 12.
07/15/2010
PDA/FDA Joint Regulatory Conference Announces Key Industry and Government Speakers
2010 PDA/FDA Joint Regulatory Conference Announces Key Industry and Government Leaders as Speakers
07/14/2010
PDA Announces Establishment of Missouri Valley Chapter
PDA Announces Establishment of New Chapter
07/11/2010
U.S. FDA Commissioner to give Keynote Presentation at 2010 PDA/FDA Joint Conference
U.S. FDA Commissioner to give Keynote Presentation at the 2010 PDA/FDA Joint Regulatory Conference
04/30/2010
Pharma Supply Chain Best Practices Identified at Manufacturer/Supplier/Regulator Workshop
Top supply chain experts representing pharmaceutical manufacturers, material suppliers, auditing companies, technology enablers, and the U.S. FDA participated in lengthy, brainstorming sessions. The Parenteral Drug Association and the U.S. FDA collaborated to develop a workshop that would facilitate various stakeholders clarifying the problems and identifying practical actions.
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