ComplianceOnline Announces Seminar on Regulation of OTC Drug Products
Palo Alto, CA, USA (PRWEB) January 17, 2014
ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on FDA’s Regulation of OTC Drug Products. The two day seminar led by regulatory affairs expert Karl M. Nobert will be held on February 13-14, 2014 in the Houston, TX.
This two day seminar will provide tools needed to develop and produce an OTC Drug Product for marketing and sale in the U.S. and for mitigating potential enforcement risks.
For more information or to register for the seminar, please click here.
Seminar instructor Karl M. Nobert is a food and drug regulatory attorney with the law firm of Squire Sanders in Washington, DC. Mr. Nobert provides regulatory advice and counseling to both large and small domestic and international pharmaceutical companies on regulatory issues related to the U.S. Food and Drug Administration’s review and approval of new drug products. He also has considerable experience related to the regulation of biologics including cellular and genetic therapies, and veterinary drug products.
During the two day interactive seminar, Mr. Nobert will discuss U.S. Food and Drug Administration’s (“FDA”) regulation of OTC drug products. He will explain the strategies for marketing and promoting OTC drug products, and for mitigating potential enforcement risks. The seminar will give the attendees an understanding of how to identify and successfully navigate an OTC drug monograph. He will also explain the difference between the various pathways for commercializing an OTC drug product and the required elements of a compliant OTC drug label.
The seminar will be beneficial for people tasked with formulation, manufacturing, labeling, marketing and promotion, import / export of OCT drug products and responsible for overseeing a company’s regulatory strategies. It will provide valuable guidance to senior quality managers, quality professionals, regulatory professionals, compliance professionals, production supervisors, manufacturing engineers, production engineers, design engineers, contract manufacturers, importers and custom agents.
Date: Thursday, February 13 and Friday, February 14, 2014, 8.30 AM- 4.30 PM
Venue & Location: DoubleTree Suites by Hilton Houston, TX
Registration Cost: $ 1,499.00 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-650-620-3937 or email customercare(at)complianceonline(dot)com
For more information on ComplianceOnline or to browse through our trainings, please visit our website.
About ComplianceOnline
ComplianceOnline is a leading provider of regulatory compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 35,000 professionals from 9,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at http://www.complianceonline.com. ComplianceOnline is a MetricStream portal. MetricStream (http://www.metricstream.com/) is a market leader in Enterprise-wide Governance, Risk, Compliance (GRC) and Quality Management Solutions for global corporations.
For more information please contact:
A Reuben Bernard
Manager of Program Marketing
ComplianceOnline
2600 E Bayshore Rd
Palo Alto CA USA 94303
650-620-3937 phone
650-963-2530 fax
reuben(at)complianceonline(dot)com
http://www.complianceonline.com
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Tags: Announces, ComplianceOnline, Drug, Products, Regulation, Seminar