HOW TO GET YOUR COMBINATION PRODUCT APPROVED & INTO THE US MARKET
August 14 - 15, 2014 - San Francisco CA USGlobalCompliancePanel
support@globalcompliancepanel.com
Phone:8004259407
Fax:302-288-6884
This course provides a comprehensive understanding of the FDA Combination Product system. Participants receive a foundation of knowledge about the FDA Office of Combination Products, the FDA Combination Product system, Combination Product submissions, and the scientific and regulatory principles involved. Participants will learn what a Combination Product is, learn about mode of action and primary mode of action, how to prepare a Request for Designation submission, Combination Product user fees, GMP for Combination Products and how to interact with the FDA Office of Combination products. They will also learn about submissions for post-approval modifications for a Combination product. This course provides the participant the ability to understand the entire FDA Combination Product Process and how to navigate through the FDA Combination Product Process to get your Combination Product onto the US marketplace. Why should you attend? A must course for those who have Combination Products or are anticipating that they will have Combination Products. This course explains the entire FDA Combination Product system and how to navigate the FDA Combination Product system. If your concern is getting your Combination Product on the US marketplace this course is a must attend for you. Areas Covered in the Session: • Learn about the FDA Office of Combination products • Learn what a Combination Product is • Learn the FDA Combination Product Process • How to navigate the FDA Combination Product system • Mode of action and primary mode of action • How to prepare a Request for Designation • User Fees for Combination products • GMPs for Combination products • Post-Approval Modifications Who Will Benefit: • Regulatory Affairs Personnel • Research Personnel • Quality Personnel • Clinical Personnel • Manufacturing Personnel • Personnel who require an understanding of the FDA Combination Product Process Course Agenda/Outline: Day One Lecture 1: Introduction To FDA: Laws and Regulations involved Lecture 2: Definitions Lecture 3: FDA Office of Combination Products Lecture 4: What is a Combination Product Lecture 5: Examples of Combination products Lecture 6: Mode of Action and Primary mode of Action Day Two Lecture 7: Preparation of Request for Designation submission Lecture 8: User Fees for Combination products Lecture 9: GMPs for Combination Products Lecture 10: Frequently Asked Questions about Combination products Lecture 11: Lead Center Lecture 12: Post - Approval Modifications Speaker Profile: Albert A. Ghignone, MS, RAC is the CEO of AAG Incorporated. For more than 30 years his focus has been on FDA related matters in regulatory affairs, quality assurance and clinical affairs. He has expertise in dealing with all aspects of the FDA approval process for drugs, biologics, medical devices and generic drugs. He has worked in every major segment of the industry-research, quality assurance, regulatory affairs, manufacturing and clinical. He has been responsible for regulatory submissions, registrations, FDA liaison, clinical studies, compliance activities and FDA training. He also has expertise in the assessment of product and facilities for due diligence relative to FDA requirements. He lectures throughout the world on numerous FDA related matters. He is a consultant to FDA and trains FDA Field Force (those who conduct FDA inspections) on GCP, GLP and GMP). In addition to training FDA personnel Mr. Ghignone also consults/trains for Drug, Biologic and Medical Device companies, US Army HIV Research Group, NIH AIDS Group, US Army Surgical Research Group and the Naval Medical Research Group. He is a member of the Regulatory Affairs Professionals Society which elected him the 1984 Professional of the Year. He has served the society as Vice President, President and Chairman of the Board of Directors. Date, Time and Venue: Location: San Francisco Date: August 14th & 15th 2014 Time: 9 am to 6 pm Venue/Hotel: Will Be Announced Soon Want to register by Wire Transfer? Please call any of our representatives on 1800 447 9407 to help you completed the transfer. Discount: Register now and save $200. (Early Bird) Until June 20, Early Bird Price: $1,295.00 from June 21 to Aug 12, Regular Price: $1,495.00 Contact Information: John Robinson Toll free: 1800-447-9407 Fax: 302-288-6884 Email: support@globalcompliancepanel.com Website: https://www.globalcompliancepanel.com Live Chat - Online Help Desk: http://www.globalcompliancepanel.com/chat/client.php GlobalCompliancePanel NetZealous LLC 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA For More Info on This Seminar Kindly Go through the Below Link: http://bit.ly/Combination_Products To Download Seminar Boucher: http://bit.ly/combination_productsbrochure GlobalCompliancePanel Seminar Gallery: http://bit.ly/1mCjvMb