Preclinical, Regulatory, and Clinical Trial Planning 101 - Galen Data

WEBINAR 16 | Preclinical, regulatory, and clinical trial planning 101 - Galen Data Planning your pre-clinical, regulatory, and clinical trial strategy from an early stage is critical to the success of an early-stage Medtech company. ✔️ Presented by: Pre-Clinical Expert: Jack Risdahl, DVM, Ph.D. — Expert in preclinical study design, particularly for the U.S. FDA; Doctor of Veterinary Medicine, Ph.D.; participation in numerous FDA meetings to discuss submission requirements, preclinical study design, and interpretation of results. Regulatory Expert: Isabella Schmitt, RAC — Director of Regulatory Affairs at Proxima Clinical Research, Inc., a contract research organization focusing on assisting emerging medical device and biotech companies in regulatory, quality, and clinical development. Clinical Expert: Jason Krzeszak — 17 years’ experience in product development of medical devices; leads the Global Product Development Strategy team at NAMSA. ✔️ What Can You Expect from this Webinar? Come learn from our panel of industry experts. Expect to walk away with practical advice concerning these three critical areas. ✔️ Discussion Topics: How do I get started with my pre-clinical strategy? What are the regulatory challenges I should expect during the preclinical and clinical phases of development? Which partners do I need to engage to ensure success of my clinical trials? ✔️ Contact Galen Data for your healthcare connectivity needs: 👉 https://www.galendata.com/contact/