This FDA compliance webinar will discuss in detail the guidance on recognition and use of consensus standards. It will focus on the topics such as voluntary conformance, declaration review and content of declaration of conformity.
Though guidance documents are not binding, they reflect the current thinking of the FDA. Even as a guidance is being drafted, this rule still holds true prior to its release. Therefore, the need to stay updated on guidance documents that may impact your business is now more than ever.
This webinar will offer a clear overview of the points covered under FDA’s recognition and use of consensus standards and elaborates every aspect within. It will also cover parallel topics such as declaration of conformity, aligning the same with ISO, limitations of consensus standards and more.
Why Should You Attend:
In 2007, FDA published an update to the guidance entitled “Recognition and Use of Consensus Standards”. The version it replaced was issued in June, 2001. As with any guidance, for those in the industry, it is important to delve deeper and understand the nuances surrounding it.Though guidance documents are not binding, they reflect the current thinking of the FDA. Even as a guidance is being drafted, this rule still holds true prior to its release. Therefore, the need to stay updated on guidance documents that may impact your business is now more than ever.
This webinar will offer a clear overview of the points covered under FDA’s recognition and use of consensus standards and elaborates every aspect within. It will also cover parallel topics such as declaration of conformity, aligning the same with ISO, limitations of consensus standards and more.
Areas Covered in the Webinar:
- Background of the guidance
- Procedures for the use of consensus standards
- General usage
- Voluntary conformance
- Declaration review
- Content of “Declaration of Conformity”
- How does this align with ISO?
- Limitations of consensus standards
- Recognition of consensus standards
Who Will Benefit:
This webinar will benefit the following personnel in the medical device industry:- Regulatory managers
- Project managers
- Staff involved with regulatory filings
- Product development managers
Course Provider
Cheryl Wagoner,