On-Demand Webinar

Tips for Accelerating Your Medical Device through the Product Lifecycle

Successfully advancing new drugs and life-saving therapies to market for emerging pharma and biotech organizations, involves complex challenges throughout the product development lifecycle. 75% of medical device companies fail and may incur up to $100B in adverse quality costs associated with correcting compliance and regulatory issues.

This webinar discusses key medical device lifecycle product development processes as well as recommends proven strategies for early-stage biopharma companies to achieve successful outcomes.
Join the webinar for critical insights to accelerate your medical device throughout the product development lifecycle. Explore the latest strategies with Alethea Wieland, President & COO of Clinical Research Strategies and Managing Expert, Advarra Consulting.

Learning Objectives:

  • Gain an in-depth understanding of the Clinical Evidence Generation Process
  • Learn successful strategies for meeting medical device regulatory requirements
  • Understand the importance of developing a proactive quality strategy
  • Gain tips for setting up emerging companies for success

Presented By


Alethea Wieland
President and CEO, Clinical Research Strategies
Advarra Consulting

R. Michael Tuttle


IRB Chair and Chief of Endocrinology Service
Memorial Sloan Kettering Cancer Center


David Weber


Associate Chief Medical Officer & IRB Chair
University of North Carolina


Hallie Kassan


Director of Human Subjects Protection
MD Anderson Cancer Center


Who should watch?

This content applies to growing medical device life science companies as well as sponsors and CROs at emerging biopharma and pharma companies. It also contains relevant insight for early-stage companies, biologics, emerging biotech companies, and anyone involved at any product development stage in advancing medical devices to market.

CE Credits

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.

This event may qualify for continuing education (CE) credits. Please check with your professional organization(s) to determine whether the event meets their CE eligibility requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: September 29, 2022
Time: 1 pm ET | 10 am PT
Duration: 1 hour

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