The FDA Drug Development Process: GLP, GMP and GCP Regulations
This Video provides an overview of the FDA's Drug Development Process. This webinar also includes the major FDA regulations involved in the Drug Development Process - the GLP, GMP and GCP regulations.
This Video is ideal for those who are new to the Drug Development process and those experienced researchers that need an update on FDA requirements. This webinar will address the basic Drug Development Process, nonclinical trials and human clinical trials. In addition the two major FDA submissions during Drug Development will be covered - the IND submission and the NDA submission.
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Organization: NetZealous BDA GlobalCompliancePanel
Website: www.globalcompliancepanel.com/
Email: support@globalcompliancepanel.com
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Пікірлер: 28
This course will help me immensely in organizing my project from A to Z.
Extremely clear, concise overview of the FDA drug approval process. Thank you!
Fabulous course. Thanks for making it available online.
Amazing session, every slide is perfect. Loved the speaker...thank you very much.
Very Informative Course! Thank you for the information
Very informative! Although a brief review, this was full of great information
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What a complex protol(s) to follow!!!!! excellent information and clinically sound, thank you!!!!!
Excellent presentation. Thank you!
A really excellent webinar thanks for putting it online. Great
@globalcompliancepane
6 жыл бұрын
Thanks sharon
Very informative.. Thank you so much for sharing this fruitful information
Excellent webinar. Please put more if possible
Thanks for the information
Thank you for your information. I learned, understand well
Thank you, I learned a lot from this webinar
can the pdf be downloaded from anywhere?
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@globalcompliancepane
6 жыл бұрын
Thanks Adedokun
To whom is this presentation dedicated? Is it for pharmacology students?
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