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Building Quality (Agreements) into Your FDA-Regulated Product: Part 2
Thursday, April 29, 2021 | 1:00 pm - 2:00 pm EDT

Alan G. Minsk, AGG's Food & Drug team leader, and Michael E. Burke, co-chair of AGG's Pharmaceuticals & Biotechnology industry team, will present a webinar as a continuation of their 2017 webinar on drafting quality agreements with third-party companies, as well as FDA enforcement in the quality agreement area.

In this webinar, Alan and Mike will discuss:

• FDA expectations
• Explore common areas of potential dispute between contract manufacturers and the sponsoring companies and practical tips to address these issues
• Evaluate ways to minimize regulatory risk and business conflicts
• Minimizing conflicts between quality agreements and related agreements

There will be an opportunity for Q&A at the end of this webinar.

Credits: AGG has applied for 1 hour of Continuing Legal Education (CLE) credit by the State Bar of Georgia for this webinar.

Apr 29, 2021 01:00 PM in Eastern Time (US and Canada)

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The legal insights discussed in this webinar include a general summary of recent legal developments. The webinar is provided for general information only, and is not intended to be, and should not be relied upon as, legal advice. Registering for a webinar is an agreement to attend the webinar, but it is not a contract for legal advice, nor does it give rise to an attorney-client relationship between AGG and any attendee. No attendee should act or refrain from acting on the basis of information exchanged in this webinar, including any answers to specific legal questions posed to the speakers, without first seeking legal advice in the relevant jurisdiction and after a full disclosure of facts applicable to the attendee’s unique situation.  Under professional rules, this webinar may be considered advertising material.