DIA会员及用户请点击登录

登录

忘记用户 ID? or 忘记密码?

Not a Member?

创建账户并加入。

Walter E. Washington Convention Center

2025 年 06 月 12 日 1:00 下午 - 2025 年 06 月 12 日 4:00 下午

801 Allen Y. Lew Place, NW, Washington, DC 20001-3614, USA

Regulatory Strategy Development for Complex Devices and Combination Products

This is a virtual pre-meeting Short Course in conjunction with the DIA Global Annual Meeting.

Instructors

James  Wabby, MHS

James Wabby, MHS

Global Head, Regulatory Affairs, Emerging Technologies and Combination Products, AbbVie, United States

James Wabby is the Global Head, Regulatory Affairs - (CoE) Emerging Technologies, Devices, and Combination Products at AbbVie in Irvine, California. He has 25 years of experience in increasing quality compliance and regulatory affairs responsibilities within the GxP regulated environment pertaining to Nutritional, Cosmetic, Branded Pharmaceutical, Generic, Biologic, Medical Device and Combination Product areas. James received his undergraduate and graduate degrees from Duquesne University and received his Health Care Compliance Certificate from Seton Hall University Law School. He is a member of various regulatory and quality work groups including RAPS, OCRA and the ASQ Orange Empire Section.

Carolyn  Dorgan, MS

Carolyn Dorgan, MS

Vice President, Solutions Engineering, Sutton's Creek, United States

Carolyn Dorgan has 15+ years experience in the medical device and combination product industries, including seven years at the US Food and Drug Administration (FDA) leading the Infusion Devices team. She currently serves as one of the Directors of Technical Services at Suttons Creek helping companies in the combination product space solve challenging regulatory, quality and organizational challenges. She implements practical solutions using her multi-disciplinary background of engineering, software, cybersecurity, human factors and business. Carolyn has a BS in Biomedical Engineering from the University of Minnesota and an MS in Technology Commercialization from the University of Texas.

Jerzy  Wojcik

Jerzy Wojcik

VP, Regulatory & Quality Services, EdgeOne Medical, United States

Jerzy Wojcik is VP of Quality and Regulatory Affairs Services at EdgeOne Medical Inc., and has over 25 years of industry experience in quality and regulatory affairs. His expertise includes identification and execution of regulatory activities across all stages of product development and lifecycle management necessary to support Class I, II and III (in both US and EU) medical device, device-biological and device-drug combination products, including wearable sensors and mobile medical applications. Jerzy has a BA in Biology, Medical Technology and Cytotechnology, was an Adjunct Professor in the School of Law at Northwestern University, is a member of RAPS, volunteers with various innovation organizations and speaks Polish and Spanish.

获得信息并保持参与

不要错失任何机会——请加入我们的邮件列表,了解DIA的观点和事件。