All ComplianceOnline seminar Events (14)

Marketing Your Medical Device - From Conventional Ads to Referral Marketing and Social Media: One and a Half-day In-person Seminar

September 19, 2013 at 8:30am to September 20, 2013 at 1:30pm – Grand Hyatt San Francisco This seminar will help medical device marketing professionals to better understand the myriad statutes and regulations that confront and impact their business. It will provide a comprehensive look at… Organized by ComplianceOnline | Type: seminar
Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations: One and a Half-day In-person Seminar

September 19, 2013 at 8:30am to September 20, 2013 at 11pm – Minneapolis This seminar and workshop will review the applicable dietary supplement regulations, walk you through real-life case studies, help you address compliance, and tell you how to respond to an enforcemen… Organized by ComplianceOnline | Type: seminar
Food Marketing Claims: Risks of Enforcement Actions and Class Action Lawsuits, Defense Strategies and Best Practices: One and a Half-day In-person Seminar

September 19, 2013 at 8:30am to September 20, 2013 at 1:30pm – Minneapolis Marriott City Center Marketing claims that promote the nutritional value, ingredient quality, and health-related benefits of food have increased significantly in recent years because of consumer expectations and competit… Organized by ComplianceOnline | Type: seminar

Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions: One and a Half-day In-person Seminar

September 18, 2013 at 8:30pm to September 19, 2013 at 12:30pm – Courtyard Philadelphia Downtown Course Description: Every company regulated by the U.S. FDA establishes procedures, practices and an internal monitoring system all designed to both meet the regulations and manage inspections. Howev… Organized by ComplianceOnline | Type: seminar

Drug Law: Understanding the Essentials of FDA's Authority over Innovative and Generic Pharmaceuticals: 2-day In-Person Seminar

September 11, 2013 at 8:30am to September 12, 2013 at 4pm – Courtyard Philadelphia Downtown Course Description: FDA authority over both innovative and generic pharmaceuticals is not only pervasive, but imposes duties on industry that, if not followed, expose drug companies and their officia… Organized by ComplianceOnline | Type: seminar

How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings: 2- day In-person Seminar

September 5, 2013 at 8:30am to September 6, 2013 at 3:30pm – Courtyard Washington, DC/U.S. Capitol Course Description: Despite a few guidance documents to help sponsors prepare for meetings with the FDA, it is a challenge to understand the most efficient and productive ways to strategize, prepare,… Organized by ComplianceOnline | Type: seminar

Analytical Instrument Qualification and System Validation: 2- day In-person Seminar

August 29, 2013 at 8:30am to August 30, 2013 at 4:30pm – Courtyard Marriott Boston - Cambridge Course Description: Analytical instruments should be qualified and systems should be validated to demonstrate suitability for the intended use. This two day in-person seminar will provide attendees t… Organized by ComplianceOnline | Type: seminar

GMP Compliance for Quality Control and Contract Laboratories

August 26, 2013 at 8:30am to August 27, 2013 at 4:30pm – Residence Inn San Diego Downtown/Gaslamp Quarter Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market… Organized by ComplianceOnline | Type: seminar

Latin America: Regulatory Compliance Requirements for Life Science Products

August 22, 2013 at 8am to August 23, 2013 at 4:30pm – Courtyard Philadelphia Downtown his two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and… Organized by ComplianceOnline | Type: seminar

Process Validation for Medical Devices

August 21, 2013 at 8am to August 22, 2013 at 5pm – Courtyard Marriott Boston ,MA 02139, USA Medical device manufacturers can avoid FDA Warning Letters, 483s and enforcement actions with a good understanding process validation principles. But knowing how to proceed is the toughest task as no… Organized by ComplianceOnline | Type: seminar