- Value of Standards throughout the Total Product Life Cycle
- Challenges and potential ways to address the hurdles
- Overview of the Regulatory Environment and it’s Relationship with Standards
Standards – Fact, Fiction or Fad?
This event will help you to learn what the value of standards are including how and when to engage in the development and use of the standards.You will hear some examples of best practices as well as Faux pas’s.You will learn about the various types of standards and what being involved brings you.You will hear about potential tools and the value of relationships and communications in the standards world.
Webinar
Jan 01 2026, Thursday
01:00 PM EDT
60
Minutes
Intermediate Level
Code: GRC0000141
- Medical Device
- Business Leaders
- R&D
- Quality and Regulatory Leader
As regulations get more complex and technologies are changing at a rapid rate, it’s important to find ways to support all stakeholders to medical devices by getting your products to market quickly in a safe and effective manner. The stakeholders include OEM Technical Personnel, Clinicians (Users), Patients, and Regulators. Each of these roles brings their expertise to the table and if you don’t understand how and when to use a standard, you aren’t serving yourself and the other stakeholders.
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