2-Day In-Person Workshop (August 25-26, 2015)
Latest Developments Affecting Non-Prescription Drugs
OTCs and consumer health care products have been a long time economic staple of both U.S. and international health care markets. However, in this age of health care reformation which calls for both cost savings and efficiencies worldwide, OTC drug products may take on an even greater role in the global health care marketplace. This hands-on working group will provide you with an essential overview of the laws and regulations covering OTC products in the U.S. and new legislation that can impact these products. It will also set the stage for helping you thoroughly comprehend the complexities of and challenges associated with this class of drug product.
Who Will Benefit:
Regulatory Affairs managers and associates, QA managers, OTC Drug Marketing managers & associates, product managers, and anyone interested in learning about U. S. OTC Drug labeling requirements.
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: firstname.lastname@example.org