CNYBAC Concept to Commercialization Virtual Series Presents: Medical Device Research, Regulations, and Path to Market

Date

Dec 08 2022

Time

3:00 pm - 4:00 pm

Medical Device Research, Regulations,
and Path to Market  

December 8, 2022, 3:00 – 4:00 p.m. 

Kathi Durdon, CCRP, Executive Director, CNY Biotech Accelerator, Upstate Medical University

Register in advance for this meeting:
https://upstate.zoom.us/meeting/register/tJcvc–trD8iEtBWSH0s-c0w4t_fzaaFl4sn  https://upstate.zoom.us/meeting/register/tJcvc–trD8iEtBWSH0s-c0w4t_fzaaFl4sn 
After registering, you will receive a confirmation email containing information about joining the meeting. 

This presentation will include an overview of medical device regulations and how risk plays a prominent role in product development, research and regulatory submission and will include an overview of regulatory history, device classification, scientific evidence, premarket submission and postmarket surveillance. 

Kathi is Executive Director of the Central New York Biotech Accelerator (CNYBAC), a 52,000+ square foot state-of-the-art multi-use facility located in Syracuse, NY.  CNYBAC, a NYS Certified Business Incubator operated by SUNY Upstate Medical University, licenses wet labs to accepted startup companies commercializing biotech technology.  Kathi manages facility operations, business development, client resource matching, grant submission, and program development such as the annually-held grant supported Medical Device Innovation Challenge, now in its 6th year.  Kathi mentors and provides resource matching services to early stage biotech innovation teams and clients regarding FDA regulations, clinical trials and state-based innovation assets available to assist commercialization needs.  Kathi serves as a Board Member for both MedTech, New York State’s biomed trade organization, and the Business Incubator Association of New York State (BIANYS) and is an Adjunct Assistant Professor at Upstate Medical University.  Kathi is a  Good Clinical Practice (GCP) Regulatory Certification Instructor and Device Conference Chair for the Society of Clinical Research Associates (SOCRA).  Ms. Durdon previously was the Director of Clinical Trials at SUNY Upstate Medical University and then managed the Clinical Affairs team at Welch Allyn, a medical device manufacturer now owned by Baxter.    

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