The FDA Drug Development Process: GLP, GMP and GCP Regulations

  Рет қаралды 97,638

GlobalCompliance Panel

GlobalCompliance Panel

8 жыл бұрын

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.
For More Information Contact -
Organization: NetZealous BDA GlobalCompliancePanel
Website: www.globalcompliancepanel.com/
Email: support@globalcompliancepanel.com
Help us caption & translate this video!
amara.org/v/JGhy/

Пікірлер: 28
@genekim1426
@genekim1426 3 жыл бұрын
Extremely clear, concise overview of the FDA drug approval process. Thank you!
@AbbyGhignone-yy7yt
@AbbyGhignone-yy7yt Жыл бұрын
I miss you papa. I love you. You’re amazing.
@jenellecotter6960
@jenellecotter6960 8 жыл бұрын
Fabulous course. Thanks for making it available online.
@michaelbui6088
@michaelbui6088 6 жыл бұрын
Very Informative Course! Thank you for the information
@curriemaria5346
@curriemaria5346 8 жыл бұрын
This course will help me immensely in organizing my project from A to Z.
@KeepRowing247
@KeepRowing247 5 жыл бұрын
Very informative! Although a brief review, this was full of great information
@MrNanobh
@MrNanobh 5 жыл бұрын
Excellent presentation. Thank you!
@shameembanu1987
@shameembanu1987 4 жыл бұрын
Amazing session, every slide is perfect. Loved the speaker...thank you very much.
@sharonwhite1298
@sharonwhite1298 6 жыл бұрын
A really excellent webinar thanks for putting it online. Great
@globalcompliancepane
@globalcompliancepane 6 жыл бұрын
Thanks sharon
@kevinkane6418
@kevinkane6418 3 жыл бұрын
What a complex protol(s) to follow!!!!! excellent information and clinically sound, thank you!!!!!
@ysshaikali1643
@ysshaikali1643 11 ай бұрын
Thank you for your information. I learned, understand well
@samirashaikh1180
@samirashaikh1180 3 жыл бұрын
Very informative.. Thank you so much for sharing this fruitful information
@user-gl2ux3dr1j
@user-gl2ux3dr1j 6 ай бұрын
Thanks for the information
@fadumaali5738
@fadumaali5738 Жыл бұрын
Thank you, I learned a lot from this webinar
@sujiths1452
@sujiths1452 4 жыл бұрын
Excellent webinar. Please put more if possible
@animesquad9046
@animesquad9046 6 жыл бұрын
it's was very amazing things ever
@globalcompliancepane
@globalcompliancepane 6 жыл бұрын
Thanks Adedokun
@caffienetime
@caffienetime 6 жыл бұрын
can the pdf be downloaded from anywhere?
@deoxyri5346
@deoxyri5346 4 жыл бұрын
To whom is this presentation dedicated? Is it for pharmacology students?
@parveshthakur2979
@parveshthakur2979 2 жыл бұрын
Can i Get this course certification
@jerrylee2698
@jerrylee2698 Жыл бұрын
arrest the medical mafia
21CFR Part 58   The Good Laboratory Practices GLP Regulation
1:13:50
GlobalCompliance Panel
Рет қаралды 14 М.
21 CFR, Parts 210 and 211
1:12:03
Compliance Insight
Рет қаралды 25 М.
НРАВИТСЯ ЭТОТ ФОРМАТ??
00:37
МЯТНАЯ ФАНТА
Рет қаралды 1,3 МЛН
Looks realistic #tiktok
00:22
Анастасия Тарасова
Рет қаралды 105 МЛН
Clinical Trials Overview: Phrases and Phases of a Clinical Trials
1:01:14
Auditing Analytical Laboratories for FDA Compliance
1:51:49
GlobalCompliance Panel
Рет қаралды 15 М.
Introduction to Module 6 with Dr. William Zamboni
19:03
NIH Clinical Center
Рет қаралды 46 М.
FDA Approval Pathways 101
1:29:00
Alliance for Health Policy
Рет қаралды 6 М.
GCP webinar
47:08
WhitehallTraining
Рет қаралды 25 М.
Understanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans
1:29:36
GlobalCompliance Panel
Рет қаралды 11 М.
Understanding New Drug Applications (NDAs)
1:00:47
Rho
Рет қаралды 26 М.
WEBINAR:  Patenting of Medical and Biotech Inventions
1:01:48
Medical Devices - ISO 14971 : Risk Management
1:12:06
GlobalCompliance Panel
Рет қаралды 28 М.