Diane Minear joins the firm as Vice President for Medical Devices. She is an experienced regulatory professional with a broad range of regulatory experience including eight years at FDA in CDRH’s Office of Device Evaluation where she was a Branch Chief for the Plastic and Reconstructive Surgery Devices Branch. Diane also worked for several medical device manufacturing companies over the past fifteen years, gaining invaluable experience in overseeing the regulatory process for medical devices, not only in the USA, but also in Europe and other major markets. “With the demand we’re seeing from the medical device industry, we’re thrilled to bring someone on board who can offer so much to our clients. Diane’s experience with both the FDA and industry will prove invaluable,” said Matthew Weinberg, CEO of The Weinberg Group.
“In these challenging economic times, it is especially important for companies to navigate the ever more complex regulatory process with the best possible regulatory strategy. The Weinberg Group has a successful, 25-year history of supporting industry and I’m excited to join the firm,” said Diane Minear, Vice President.
Ms. Minear has led multiple training sessions for regulatory professionals at RAPS and other professional meetings over the past 15 years while serving in leadership roles at Codman, a Johnson & Johnson company, MedaSorb International, and Smith & Nephew Endoscopy. She holds a B.S. in Nursing and is quick to both recognize and emphasize the clinical perspective of devices in the regulatory process.
The Weinberg Group solves critical business problems leveraging the talent of an elite team of scientists. As a multinational scientific and regulatory consulting firm, we help companies resolve complex issues surrounding science, management, law and regulation. Since 1983, we have been committed to helping our clients address regulatory requirements, improve manufacturing processes and support products in the legal system, the media and in the court of public opinion.
