12th Annual FDA/AdvaMed Medical Devices and Diagnostics Statistical Issues Conference – April 24-25, 2019 in Washington, DC
This annual conference brings together leading authorities from FDA, industry and academia to address the latest statistical trends and issues facing medtech organizations. This conference allows attendees to take a deeper dive into either therapeutic [...]
Seminar – Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) – New Orleans, LA – May 2-3, 2019
This 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 renewals across Pharmaceuticals, Biologics, Medical Devices and Combination Products. The Course [...]
Process Validation Requirements and Industry Practice Course – April 16-18, 2019 in Arlington, VA
This 2.5-day course provides attendees with practical tools and techniques for process validation requirements for FDA’s Quality System regulation and recognized Process Validation Guidance from the Global Harmonization Task Force. The program includes industry best [...]
The Quality System Regulation 21 CFR 820 ANSI/AAMI/ISO 13485: Navigating Requirements – April 8-12, 2019
For registration info: https://www.aami.org/events/eventdetail.aspx?ItemNumber=7186