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Jul 2015


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The Future of OTC Drug Regulation and the Monograph Process

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This training program will offer attendees a comprehensive understanding of how OTC drug products are regulated in the U.S. It will also help differentiate the various pathways for commercializing an OTC drug product and suggest take away strategies for marketing and promoting OTC drug products.

Why Should You Attend:
Go into any CVS Retail Pharmacy, Wal-Mart, Meijer Grocery Store, Rite Aid Retail Pharmacy or Target in the United States and you are guaranteed to find store shelves lined with hundreds or even thousands of different OTC drug products. Some of the most recognized OTC drug products include ibuprofen tablets, anti-itch creams, nasal decongestant sprays, cough syrups, antacids, allergy medicines and topical pain relievers.

Who Will Benefit:
This course is designed for people tasked with developing and maintaining an animal health company’s product portfolio; and for those responsible for overseeing a company’s regulatory strategies. This includes individuals responsible for overseeing regulatory affairs, developing strategies for obtaining veterinary drug product approvals and those tasked with ensuring corporate compliance. Among others, this includes:
Quality professionals
Regulatory and compliance professionals
Production supervisors and engineers
Manufacturing engineers
Design engineers

Instructor Profile:
Karl M. Nobert focuses his practice on the representation and counseling of clients in the food and drug industry including advising clients on matters related to the regulation of human prescription and nonprescription drugs, human and veterinary biological products including regenerative medicine, medical devices, food and dietary supplements.

Use coupon code 232082 and get 10% off on registration.

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