510 (k) Applications- Medical Devices Software - 0 views
-
Online Compliance on 02 Mar 15This webinar will discuss the structure and level of detail required in filing a 510k, when a medical device is software or contains software.
Group items tagged
Rules and Regulations for Advertising & Marketing in Canada - 0 views
-
Attend this upcoming webinar to be aware of strict rules and regulations for advertising medical, pharmaceutical devices and natural health products in Canada.
FDA Regulations for Importing-Exporting Medical Devices - 0 views
-
Attend this webinar to understand how to better manage your import and export compliance activities and help support your logistics supply chain.
eMDR Final August 14, 2015-eMDR Final Rule - 0 views
-
Learn about the FDA published final rule on Electronic Medical Device Reporting so that your company can be ready, and the requirements for submitting MDR reports electronically
Risk Management Tool: Risk Analysis - 0 views
-
Webinar on various terms used in risk management and importance of ISO 14971 & ISO 13485 in risk management during the life cycle of medical devices.
Investigational Product Accountability -Online Training - 0 views
-
Learn to maintain accurate records and accountability of investigational products associated with premarket clinical studies.
Equipment Validation-FDA Standards - 0 views
-
Get trained on practical aspects of FDA process validation, equipment qualification, Data analysis, statistical tools for Process Quality Management, more.
FDA Compliance-FDA Regulated Computer System Projects - 0 views
-
Learn about the best planning approach for guaranteeing foremost business edges and achieving Food and Drug Administration compliance through this webinar.
Product Quality Reviews - FDA, EU and Canada Regulatory Requirements - 0 views
-
Attend this webinar to understand the world-wide regulatory requirements for Annual Product Reviews. Know the regulations governing product review.
1 - 9 of 9
Showing 20▼ items per page