Bernadette Attinger

Bernadette Attinger has extensive experience in regulatory affairs, spanning across multiple pharmaceutical companies. Bernadette began their career in 2001 at Teva Pharmaceuticals as an SR Regulatory Affairs Associate, where they managed and reviewed drug applications and provided regulatory support. In 2005, they moved on to Braun Medical as a Regulatory Affairs Manager, where they played a leading role in the development of sterile products. From 2007 to 2009, Attinger worked at Ebewe Parenta Pharmaceuticals as the Director of Regulatory Affairs, overseeing the filing and maintenance of applications. Bernadette then joined Sandoz as a Director of Regulatory Affairs, managing various teams and responsible for FDA liaison. Attinger further advanced their career at Johnson Matthey Pharma Services, taking on the role of Director of Regulatory Affairs and Quality Assurance, where they provided regulatory guidance and set up internal policies and procedures. After this, they held positions at Qualitest Pharmaceuticals and Par Pharmaceutical, where they were responsible for all regulatory activities and led the merging of the two companies. Bernadette then served as the Senior Director of Global Head of Regulatory at PuraCap Pharmaceutical before their most recent role as the Senior Director of Regulatory Affairs at Torrent Pharma Inc. Attinger currently holds the position of Vice President of Regulatory Affairs at Avet Pharmaceuticals.

Bernadette Attinger obtained a Bachelor of Science degree in Biology with a specialization in Microbiology from Bloomsburg University of Pennsylvania. However, no specific information regarding the duration of their studies or the year of completion has been provided.