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
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DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour