Explore the most recent editions of MPO Magazine, featuring expert commentary, industry trends, and breakthrough technologies.
Access the full digital version of MPO Magazine anytime, anywhere, with interactive content and enhanced features.
Join our community of medical device professionals. Subscribe to MPO Magazine for the latest news and updates delivered straight to your mailbox.
Explore the transformative impact of additive manufacturing on medical devices, including design flexibility and materials.
Learn about outsourcing options in the medical device sector, focusing on quality, compliance, and operational excellence.
Stay updated on the latest electronic components and technologies driving innovation in medical devices.
Discover precision machining and laser processing solutions that enhance the quality and performance of medical devices.
Explore the latest materials and their applications in medical devices, focusing on performance, biocompatibility, and regulatory compliance.
Learn about advanced molding techniques for producing high-quality, complex medical device components.
Stay informed on best practices for packaging and sterilization methods that ensure product safety and compliance.
Explore the latest trends in research and development, as well as design innovations that drive the medical device industry forward.
Discover the role of software and IT solutions in enhancing the design, functionality, and security of medical devices.
Learn about the essential testing methods and standards that ensure the safety and effectiveness of medical devices.
Stay updated on innovations in tubing and extrusion processes for medical applications, focusing on precision and reliability.
Stay ahead with real-time updates on critical news affecting the medical device industry.
Access unique content and insights not available in the print edition of the MPO Magazine.
Explore feature articles that delve into specific topics within the medical device industry, providing in-depth analysis and insights.
Gain perspective from industry experts through regular columns addressing key challenges and innovations in medical devices.
Read the editor’s thoughts on the current state of the medical device industry.
Discover the leading companies in the medical device sector, showcasing their innovations and contributions to the industry.
Explore detailed profiles of medical device contract manufacturing and service provider companies, highlighting their capabilities and offerings.
Learn about the capabilities of medical device contract manufacturing and service provider companies, showcasing their expertise and resources.
Watch informative videos featuring industry leaders discussing trends, technologies, and insights in medical devices.
Short, engaging videos providing quick insights and updates on key topics within the medical device industry.
Tune in to discussions with industry experts sharing their insights on trends, challenges, and innovations in the medical device sector.
Participate in informative webinars led by industry experts, covering various topics relevant to the medical device sector.
Stay informed on the latest press releases and announcements from leading companies in the medical device manufacturing industry.
Access comprehensive eBooks covering a range of topics on medical device manufacturing, design, and innovation.
Highlighting the innovators and entrepreneurs who are shaping the future of medical technology.
Explore sponsored articles and insights from leading companies in the medical device manufacturing sector.
Read in-depth whitepapers that explore key issues, trends, and research findings for the medical device industry.
Discover major industry events, trade shows, and conferences focused on medical devices and technology.
Get real-time updates and insights live from the CompaMed/Medica conference floor.
Join discussions and networking opportunities at the MPO Medtech Forum, focusing on the latest trends and challenges in the industry.
Attend the MPO Summit for insights and strategies from industry leaders shaping the future of medical devices.
Participate in the ODT Forum, focusing on orthopedic device trends and innovations.
Discover advertising opportunities with MPO to reach a targeted audience of medical device professionals.
Review our editorial guidelines for submissions and contributions to MPO.
Read about our commitment to protecting your privacy and personal information.
Familiarize yourself with the terms and conditions governing the use of MPOmag.com.
What are you searching for?
Dermatologist Mary Spellman and Clinquest founder Cornelis Wortel join the governing body.
September 16, 2024
By: Michael Barbella
Managing Editor
Catawba Research has expanded its Scientific Advisory Board (SAB) with the appointments of Mary Spellman, M.D., and Cornelis (Cees) Wortel, Ph.D. The new appointments add further value to Catawba Research’s customer-centric support model and expertise in dermatology and immunology—both of which are pertinent to developing cutting-edge therapies. This enhanced expertise enables customers to better navigate the complexities of clinical trials with greater confidence, ultimately accelerating the path to market. “The addition of Spellman and Wortel to our SAB is a testament to our dedication to scientific excellence and innovation and will be invaluable in supporting the development of groundbreaking therapies. As we celebrate our company’s 10th anniversary, we continue to strengthen our position as the top choice for companies seeking a CRO with deep, specialized knowledge in these rapidly expanding areas of clinical development,” Catawba Research Chief Scientific Officer and Advisory Board Chairman Jack McLane, Ph.D., said. Spellman and Wortel are the most recent additions to Catawba Research’s team of scientific and regulatory advisors who support sponsors across various therapeutic areas and provide clinical development and regulatory strategy across North America, Europe and Asia. Spellman is a board-certified dermatologist with more than 30 years of experience in biopharmaceutical development. Her focus has been on inflammatory and infectious diseases, acne vulgaris, rare genetic skin conditions and cutaneous carcinomas. Her clinical oversight includes NDAs for topical corticosteroids, antifungals, antibiotics, retinoids, the PDE4 inhibitor crisaborole, and systemic agents for dermatologic and oncologic indications. She has also collaborated with the U.S. Food and Drug Administration to develop and validate clinical endpoints for novel indications. Spellman has held senior leadership roles at Castle Creek Biosciences, Menlo Therapeutics, Revance Therapeutics, Biogen Idec, Connetics Corporation, and Novartis, providing clinical leadership for numerous global regulatory submissions. She has served on the Board of Directors and as president of Dermatologists in Industry, on the Board of Directors for Women’s Dermatology Society, and as associate editor for the Journal of the American Academy of Dermatology. Spellman earned her medical degree from the Medical College of Wisconsin and is a diplomate of the American Board of Dermatology and a fellow of the American Academy of Dermatology. Dr. Wortel is a senior executive with more than 25 years of experience and has a proven track record in designing and implementing clinical development plans and regulatory strategy. His expertise spans a wide range of indications with a focus on autoimmune and immuno-oncology indications. After earning his medical degree and doctorate in immunology research at the University of Amsterdam, Dr. Wortel joined Centocor as a clinical team leader to develop Remicade. He most recently served as chief medical officer at Bingli and has held senior consulting leadership roles at Critical Therapeutics, Aegerion Pharmaceuticals, Galapagos, and Molecular Partners AG. Dr. Wortel is a venture partner at Vesalius Biocapital III, has chaired and presented at regulatory agency meetings in both the United States and Europe, and has extensive experience in digital health, data science, real-world data, and artificial intelligence/machine learning. Catawba Research is a full-service contract research organization (CRO) providing clinical management expertise and services. Its executive leadership team has more than 160 years of combined experience and is comprised of industry professionals from large global pharmaceutical, small- and medium-sized biotechnology, global full-service CRO, and eClinical technology backgrounds. Its cross functional team of clinical trial professionals have successfully supported 800-plus clinical trials across their careers and since 2014, the company’s work has delivered 33 regulatory agency approvals. As an international service provider, Catawba Research is headquartered in North Carolina, and Mumbai, India. Its service offering also includes a Site Management Organization (SMO) based in Texas.
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !