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FDA’s Revocation of Mutual Recognition Regulations

$9.99

Gain comprehensive insights into the FDA’s proposed rule to revoke regulations on mutual recognition of pharmaceutical and medical device reports with the European Community. Learn about the impact of the 2017 Amended Pharmaceutical Annex, reasons for revocation, and implications for industry practices.

In this course you will learn the following:
* Understand the purpose and intent behind the proposed revocation of part 26.
* Recognize the major provisions and legal authority of the proposed rule.
* Identify the potential impacts and benefits of the rule change.

NOTE: Unless otherwise indicated, all course purchases are for access to the course for a period of 1-year.  At the end of the one year term, the course will be set to “inactive”. 

Why This Course is Important
Without this course, you’ll miss crucial updates on the FDA’s regulatory changes that affect international pharmaceutical and medical device practices, potentially impacting compliance and operational strategies.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Revocation of Regulations Regarding the Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and The European Community.

Key regulatory references include:

Course SKU
FR-24-219-1