結果 : clinical study report guidelines fda
31:16

FDA Guidance on Conduct of Clinical Trials of Medical Products During the Public Health Emergency

U.S. Food and Drug Administration
1,953 回視聴 - 3 年前
3:54

The Four Phases of Clinical Trials | Diversity in Clinical Trials | AKF

kidneyfund
769,350 回視聴 - 2 年前
54:21

Most Common Issues with CDISC-SEND Data in FDA Toxicology Review – Sep. 12, 2019

U.S. Food and Drug Administration
5,726 回視聴 - 4 年前
41:00

FDA Regulatory Requirements for Clinical Investigators and Case Examples (9of14) REdI 2018

U.S. Food and Drug Administration
4,113 回視聴 - 4 年前
53:23

FDA Webinar on the Infant Formula Transition Plan for Exercise of Enforcement Discretion (Part 1)

U.S. Food and Drug Administration
2,792 回視聴 - 2 年前
23:44

Regulatory and Clinical Trials for Therapeutics

Fast Forward Medical Innovation – Commercialization Education
1,431 回視聴 - 9 年前
54:27

June 17, 2021- Introduction to FDA: History, Regulations, and Clinical Trial Design

UCSF Pediatric Grand Rounds
2,118 回視聴 - 3 年前
39:09

Walkthrough of an FDA Clinical Investigator Site Inspection (12/14) REdI 2017

U.S. Food and Drug Administration
6,279 回視聴 - 4 年前
17:28

Everything You Need to Know About the RSV Vaccine and Antibody

PedsDocTalk TV
182 回視聴 - 2 日前
21:20

Investigator Responsibilities - Safety Reporting for Investigational Drugs and Devices

U.S. Food and Drug Administration
2,217 回視聴 - 3 年前
35:16

Overview of Postmarketing Drug Safety Reporting Requirements - REdI 2020

U.S. Food and Drug Administration
6,134 回視聴 - 4 年前
46:41

FDA EMA immunogenicity guidelines APR2020

maria-dolores vazquez-abad
2,788 回視聴 - 4 年前
6:38

What is Safety Reporting in Clinical Trials?

GCP-Mindset - All About Clinical Research
2,818 回視聴 - 1 年前
1:26:22

FDA Study Data Technical Rejection Criteria (TRC): What you need to know!

U.S. Food and Drug Administration
4,639 回視聴 - 3 年前
1:26:23

Diversity in Clinical Trials: Learn about Enrollment Trends and Resources from FDA

U.S. Food and Drug Administration
7,848 回視聴 - 3 年前
1:01:49

Industry Panel Insights on FDA's Guidance and Inclusive Clinical Trials

Stanford CME
152 回視聴 - 8 か月前
53:25

OTC Monograph Reform: OMOR Format and Content & Electronic Submissions

U.S. Food and Drug Administration
1,396 回視聴 - 1 年前
4:10

Serious Adverse Event Reporting for Investigators

GCP-Mindset - All About Clinical Research
6,669 回視聴 - 2 年前
51:57

Webinar — Comparing CTA Submission (EMA/Health Canada) to IND Applications (FDA) for Phase I Trials

Altasciences
2,220 回視聴 - 3 年前

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1:09:42

FDA Study Data Technical Conformance Guide v4.4 - Nov 22, 2019

U.S. Food and Drug Administration
6,201 回視聴 - 4 年前