Search result for Regulatory affairs Online Courses & Certifications
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Drug Regulatory Pathways, Data and Market Exclusivity US AU
by Abhishek TONGIA- 4.4
1 hour on-demand video
This course provide brief overview of different regulatory pathways along with data and market exclusivity for drug registration in US and Australia (AU) region for prescription (Rx) and over the counter (OTC) medicines. This course is beneficial for regulatory affairs, quality assurance, R&D professionals who would like to start their career in US and AU regulatory domain of healthcare or pharmaceutical company ....
$54.99
Practical Regulatory Affairs 2020 - European Medical Devices
by Pubudi Silva- 4.2
1.5 hours on-demand video
Written and developed by a group of Regulatory Affairs professionals currently working in industry, this course focuses on the most common issues and questions we receive from medical device manufacturers looking to transition to the MDR....
$11.99
Good Clinical Practice (ICH GCP) for Clinical Research
by Dr. Leire Zuñiga- 4.1
1.5 hours on-demand video
A course designed not only for investigators and site staff but also its content is key for CRAs, Clinical Operations staff, Clinical QA, and Regulatory Affairs departments. Comprehend the key ICH-GCP requirements and regulatory expectations regarding conduct of clinical trials...
$14.99
U.S. Public Policy: Social, Economic, and Foreign Policies
by Thomas E. Patterson- 0.0
4 Weeks
We’ll examine partisan divisions over regulatory policy, and the basis for those divisions. The partisan divisions over regulatory policy and the basis for those divisions...
$99
Introduction to Compliance Risk Management CRM
by Usman Zuberi- 4.2
1.5 hours on-demand video
How companies manage risk of non compliance to regulatory requirements? In this course you will get insight about how the companies and regulators are focusing on strong compliance culture to manage the affairs of the company or institutions and avoid penalties and reputation losses....
$12.99
Drug Development
by Williams S. Ettouati, Pharm.D. , Joseph D. Ma- 4.7
Approx. 10 hours to complete
All data generated about the small molecule or biologic is collected and submitted to the regulatory authorities in the US at the FDA, Food and Drug Administration FDA, in Europe the EMA or European Medicines Agency, Japan Ministry of Health and other countries which may require their own national approvals. Regulatory Considerations When Filing an Investigational New Drug Application I...
Introduction to Satellite Communications
by Laurent Franck , Tarik Benaddi , Julien Fasson , Nathalie Thomas , Marie-Laure Boucheret- 4.6
Approx. 33 hours to complete
Mohamed Benseddik - regulatory affairs...
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