Past Events - Medical Equipment Show / Conference in Palm Beach, FL USA
Drug accountability in clinical trials - Is your site GCP compliant?
This webinar on Drug accountability in clinical trials will provide understanding of how to conduct compliant and successful clinical trials by..
Pediatric Clinical Trials in the EU: Regulatory, Scientific, and Ethical Challenges
This training will cover compliance requirements for running clinical trials in pediatrics, particularly in the EU to comply with the EU ethical..
Clinical Project Management
This 6-hr Clinical Project Management training will provide valuable tools and practical tips for initiating, managing, and presenting data from..
Critical Compliance and Major Changes for the EU Clinical Trials Directive
This EU Clinical Trials Directive training will cover major changes to compliance requirements concerning the Clinical Trial Directive that you should..
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters
This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this,..
How strong is your knowledge of GCP?
This 90-minute GCP webinar will present the official GCP text instead of interpretations of the GCP guidelines. It will analyze clinical trial..
Compliance Webinar on the topic of Business, Project and Compliance Risk
Companies have been applying the techniques of ISO 14971 to product safety, but the techniques can also be applied to other risks encountered in all..
The FDA Warning Letters: Revealing the Critical Conduct Creas in Clinical Ctudies
This 90-minute webinar will review FDA warning letters in Clinical Trials and present critical parameters to watch out for in order to secure..
Purchasing and Supplier Controls in the Medical Device Industry
Why you should attend: A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA..
Mobile Medical Applications: Software Regulatory Requirements
This mobile medical apps training will outline the regulatory requirements for medical device software development processes, and the requirements..
Drug Discovery and Development
During this event, the hottest topics in Drug Discovery will be addressed in a webinar-style auditorium with the opportunity for live Q&A at the..
Effective and Compliant Health Care Marketing Program
Learn about the dos and don’ts in health care marketing activities, OIG guidance and advisory opinions with regards to marketing activities.This..
Medical Device Design Control-Medical Device Compliance
Learn how to develop medical device design controls in compliance with the federal regulations, learn about CFR 21 Part 820.
Understanding ISO 13485-FDA Requirements for Medical Devices
Understanding ISO 13485: 2015 Requirements for Medical Devices Instructor: Meena Chettiar Product ID: 500883 Description The speaker will provide the..
ComplianceOnline Medical Device Summit
Innovate novel ideas for advancements in medical device technologies without compromising their safety and effectiveness. This summit brings together..
