Marketing to the Hispanic Market

Japan's classification system differs from that of the United States or European Union Medical devices are classified to Class I, II, III, or IV depending on their risk level Medical devices must also comply with Japanese Industrial Standards and these standards define industry-wide safety and performance requirements Strict new package insert requirements Change to MAH Licensing rules A new MAH License category for In Vitro Diagnostic (IVD) devices A new registration system for manufacturers A new QMS conformity assessment system New formats for pre-market certification and pre-market approval applications Expanded scope of third party certifications Rules for software as a medical device Rules for transferring pre-market certifications And Much More...

The FDA just banned 19 active ingredients that are used in antibacterial soaps. This major regulation will have a huge impact on this multi-million-dollar industry since the FDA Rule will require companies to remove these ingredients from their products or remove the products from the market. Manufacturers will have one year to take these products off the market or reformulate them.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FDA-ACTION-ASPECTIC-WASH-PRODUCTS-501903/DECEMBER-2016-ES-TRAININGREGISTRY

After years of negotiation, an agreement was reached by the European Council's Permanent Representatives Committee and the European Parliament's Environment and Health Committee in June 2016 on the new Medical Device (MD) and in vitro Diagnostic Device (IVDD) regulations. Two documents are planned for September 2016, and the Council and Parliament could adopt them by the end of the year. The new rules will go into effect three years after publication for medical devices and five years after publication for IVDs.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/UPCOMING-EU-MEDICAL-DEVICE-501791/NOVEMBER-2016-ES-TRAININGREGISTRY

This webinar gives a clear overview of claims about food products and supplements in labeling, advertising and other forms of promotion. The material will be presented in layman's terms, so it can be understood by business and marketing executives who have no legal background. The webinar will include examples and will cover different types of products and product claims; labeling, advertising and social media, the roles of various government agencies, using testimonials, and sources of additional information.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/FDA-FTC-REQUIREMENTS-501745/OCTOBER-2016-ES-TRAININGREGISTRY

Jocelyn Samuels, the top Federal official in charge of HIPAA enforcement said, "The one critical thing covered entities and business associates must do to ensure compliance with HIPAA’s Privacy Breach, and Security Rules is a HIPAA Risk Analysis - a comprehensive and thorough approach to assessing and addressing the risks to all of the protected health information(PHI) they maintain."Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HIPAA-RISK-ANALYSIS-501472/JUNE-2016-ES-TRAININGREGISTRY

MVP Seminars LLC, is a leading nationwide provider of business training seminars, consulting professionals & exceptional coaches, with quality academic backgrounds. Largest family operated seminar company in USA. Please call 510-558-3495.

MVP Seminars LLC, is a leading nationwide provider of business training seminars, consulting professionals & exceptional coaches, with quality academic backgrounds. Affordable prices, call 510-558-3495.