Thursday, February 27, 2014

Regulatory Affairs in the USA (FDA) for Drugs and Biologics: 2-day In-Person Seminar

February 27, 2014 at 8:30am to February 28, 2014 at 4:30pm – Double Tree San Diego Downtown Course Description: This regulatory compliance training will give the participants a detailed presentation on regulatory affairs of human pharmaceuticals (drugs and biologics) in the United States to… Organized by ComplianceOnline | Type: biotech
Post Market Surveillance for Medical Devices

February 27, 2014 from 10am to 11:30am – Online Event This 90-minute webinar covers all aspects of post market surveillance (PMS) for medical devices. It will direct you to the specific documents for the detailed information you need for an effective po… Organized by ComplianceOnline | Type: medical
GMP Requirements for Validation and Re-Validation of Analytical Procedures

February 27, 2014 from 10am to 11am – Online Event This webinar will explain the cGMP and ICH validation requirements for analytical procedures and discuss key factors that would affect validation process of analytical procedures. It will review the… Organized by ComplianceOnline | Type: pharmaceutical
Webinar On - FDA’s 21 CFR Part 11 Add-on Inspections

February 27, 2014 from 12pm to 1pm – Online Description : In December 2010 the FDA began a project to better understand the industry’s adherence (or lack thereof) to 21 CFR Part 11. This involves the add on’ surveillance inspections of the spo… Organized by compliancetrainings | Type: online, training