FDA’s Regulation 2020 - "FDA’s Regulation of OTC Drug Products What It Is, How to Analyze It, Make It Work for You"
Topics/Call fo Papers
Over-the-Counter Drug Products or “OTC Drugs” include many of the well-known products that we use to treat or control the symptoms of occasional and moderate health conditions. Available without a prescription and for purchase directly off-the-shelf
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
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.
Speaker:
Karl focuses his practice in FDA Regulatory law, representing U.S. and international clients in the food and drug industries with regard to pharmaceuticals and OTC drugs,
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
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.
Speaker:
Karl focuses his practice in FDA Regulatory law, representing U.S. and international clients in the food and drug industries with regard to pharmaceuticals and OTC drugs,
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Last modified: 2020-12-07 21:50:21