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The Regulations of OTC Drugs


Thursday, October 19, 2017 at 8:30 AM - Friday, October 20, 2017 at 4:30 PM (EDT)

The Regulations of OTC Drugs

Ticket Information

Ticket Type Sales End Price Fee Quantity
Seminar One Registration (Early bird offer)
For Registrations till August 15, 2017 - $1499
Ended $1,499.00 $19.95
Seminar One Registration Oct 19, 2017 $1,699.00 $19.95
Seminar One Registration (With 2 Nights Stay) Oct 19, 2017 $1,899.00 $19.95

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Event Details

The U.S. Food and Drug Administration’s (“FDA”) is responsible for the regulation and oversight of the U.S. OTC drug market. Congress has granted FDA regulatory authority over the formulation, manufacturing, labeling, marketing and promotion; and import / export of OTC drug products into the U.S. Under this current regulatory regime, there are 3 pathways that a company may follow to enter the OTC drug market including (a) following an appropriate Drug Monograph; (b) with an Agency approved New Drug Application (“NDA”); or (c) via the currently popular Rx-to-OTC Switch Process.

This course on FDA regulation of OTC drug products is intended to provide attendees with the knowledge and skills needed to develop and produce an OTC Drug Product for marketing and sale in the U.S. Attendees will gain an understanding of :

  • Various available options for producing and selling an OTC drug product,
  • U.S. Food and Drug Administration’s (“FDA”) regulation of OTC drug products,
  • Strategic recommendations for mitigating the risk of enforcement action in the future.


Learning Objectives:

Participants who attend this course on FDA regulation of OTC drugs will:

  • Gain a comprehensive understanding of how OTC Drug Products are regulated in the U.S.
  • Learn to distinguish between a potential Rx pharmaceutical product and an OTC drug.
  • Recognize the difference between the various pathways for commercializing an OTC Drug Product.
  • Understand how to identify and successfully navigate an OTC Drug Monograph.
  • Recognize when reliance on a Proposed Rule, Final Rule and/or Drug Monograph is appropriate.
  • Understand how to determine whether an Ingredient is considered Safe or GRAS/E for use in an OTC Drug and understand the difference between Category I, II and II Ingredient designations.
  • Identify the required elements of a compliant OTC Drug Label.
  • Take away strategies for marketing and promoting OTC drug products, and for mitigating potential enforcement risks.
  • Possess a working knowledge of the Rx-to-OTC Switch Process.
  • Review and evaluate several of FDA's current OTC Monographs


For Registration -

Note: Use coupon code REFERRAL10 and get 10% off on registration.

Have questions about The Regulations of OTC Drugs? Contact ComplianceOnline

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When & Where

Jersey City

Jersey City, NJ

Thursday, October 19, 2017 at 8:30 AM - Friday, October 20, 2017 at 4:30 PM (EDT)

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