by Admin SDRAN | Jul 22, 2024 | SDRAN Events
FDA’s New Medical Device QMSR: Everything You Need to Know From an FDA & Global Expert! Program Speaker: Kim Trautman, M.S.Medical Device, IVD, andCombination Product Expert Event Agenda: DATE: Thursday, 22 August 2024 TIME: PDT – Pacific Daylight...
by Admin SDRAN | Jul 17, 2024 | SDRAN Events
Tuesday, 6 August 2024 Panel Discussion: The Current State of Laboratory Developed Tests (LDTS) and Implications of FDA’s Final Rule on the Future of LDT Testing Program Speaker: Karin A. Hughes, Ph.D. Senior Vice President of Global Regulatory & Quality at...
by Admin SDRAN | Jun 11, 2024 | SDRAN Events
Unlocking the Secrets of an Effective Medical Device Post-Market Surveillance Program: A Deep Dive into FDA Regulatory Requirements, Best Practices and Current Trends Program Speaker: Jennifer Mascioli-TudorFounder and CEOJMT Compliance Consulting Event Agenda: DATE:...
by Admin SDRAN | May 5, 2024 | SDRAN Events
Wednesday, 15 May 2024 Supplier Auditing: 10 Common Mistakes & How To Sidestep Them Program Speaker: Kellan IlsePartner at Quality Auditing LLC Event Agenda: DATE: Wednesday, 15 April 2024 TIME: 5:30 – 6:00 PM Light Dinner 6:00 – 6:05 PM ...
by Admin SDRAN | Mar 31, 2024 | SDRAN Events
Wednesday, 17 April 2024 Overview of the Drug Adverse Event Lifecycle Program Speaker: Jacqueline Wright, BSc, RNPharmacovigilance Leader Event Agenda: DATE: Wednesday, 17 April 2024 TIME: 5:30 – 6:00 PM Light Dinner 6:00 – 6:05 PM Welcome...
by Admin SDRAN | Mar 13, 2024 | SDRAN Events
EU Clinical Trial Regulation (CTR) and Clinical Trials Information System (CTIS) Program Speaker: Theresa Falls Manager of Regulatory Affairs Avidity Biosciences, Inc. Event Agenda: DATE: Wednesday, 20 March 2024 TIME: 6:00 – 6:05 PM Welcome and...
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