The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated.
This seminar will focus on addressing these concerns and educating participants on FDA’s recent medical device software regulation strategies.
Note: Use coupon code 232082 and get 10% off on registration.
For Registration - http://www.complianceonline.com/fda-medical-device-software-regulation-strategy-seminar-training-by-ex-fda-official-seminar-training-80242SEM-prdsm?channel=pickevent
Course Description: All facilities manufacturing pharmaceuticals, biologics,...
Q
Course Description: In this two day workshop conference you will learn the...
Q
Course Description: Trade Compliance plays a prominent role in international...
Q
Course Description: This course is designed to introduce to individuals the...
Q
Course Description: Risk Based Internal Auditing (RBIA) is defined by the...
Q
Course Description: FDA inspection and oversight of quality control (QC)...
Q
Aims Recently, a series of headline-grabbing operational risk incidents at...
Q
Course Description: Is your company at risk for non-compliance? Is your...
Q
Course Description: Are the financial transactions within your organization...
Q
Course Description: If an internal audit is to assess the effectiveness of the...
Q
Course Description: The objective of this two day "Essentials of USP...
Q
Global Food Supply Chain Risk ...
Q
Course Description: Raw material requirements in a cGMP environment are often...
Q
Course Description: This interactive one and a half day course led by Ms. Rita...
Q
Course Description: This seminar will cover auditing human resources practices...
Q
Course Description: Importing products regulated by the FDA has become more...
Q
Course Description: This two day seminar will focus on internal controls...
Q
Course Description: Organizations of all kinds and sizes are increasingly...
Q
Course Description: Formal written Standard Operating Procedures (SOPs) are...
Q
Course Description: If you are looking for the answer to the following...
Q
Course Description: A growing public demand for supplements has resulted in a...
Q
Course Description: Significant changes in the regulations and...
Q
Course Description: Significant changes in the regulations and industry...
Q
Course Description: Supplier selection and management is one of the critical...
Q
Course Description: This 2-day seminar is designed to assist companies that...
Q
Course Description: Naturally, getting a project to deliver on time, within...
Q
Course Description: This interactive two day seminar will cover the various...
Q
Course Description: This seminar will help you understand the regulatory,...
Q
Course Description: Regulatory professionals have to write highly technical...
Q
Course Description: This GRC Professional Seminar will teach you how to...
Q
Course Description: Bribery can often damage your business and your...
Q
Course Description: This two day course will prepare firms for a quick,...
Q
Course Description: Unlike risk management, which involves managing potential...
Q
Login to comment