結果 : fda documentation requirements
3:17

How does the FDA approve new drugs?

U.S. Food and Drug Administration
70,805 回視聴 - 2 年前
8:13

FDA's Latest Guidelines for Pharma Manufacturing | What's New?

Pharmaguideline
9,757 回視聴 - 11 か月前
10:55

Importing FDA-Regulated Products: The Import Process

U.S. Food and Drug Administration
66,120 回視聴 - 3 年前
6:52

Understanding the US FDA Drug Approval Process | Step-by-Step Explanation for Pharma Professionals

Pharmaguideline
2,611 回視聴 - 5 か月前
56:45

Managing SOP Compliance per FDA Regulations

Compliance Key
819 回視聴 - 4 年前
4:17

Comprehensive Guide to Documentation and Record-Keeping for FDA Compliance in Life Sciences

eLeaP®
449 回視聴 - 1 年前
3:48

What Are The FDA Requirements For CAPA? - How It Comes Together

How It Comes Together
8 回視聴 - 2 か月前
54:27

Software Validation Documentation for Medical Devices - FDA eSTAR

Medical Device Academy
3,219 回視聴 - 1 年前
5:50

EU GMP vs FDA cGMP Key Differences

Pharmaguideline
4,232 回視聴 - 10 か月前

-
3:32

About FDA’s Data Standards Program

U.S. Food and Drug Administration
5,878 回視聴 - 8 年前
1:18:51

Introduction to U.S. FDA Medical Device Regulations

Registrar Corp
839 回視聴 - 5 か月前

-
6:05

FDA Inspection and Compliance : Regulatory Requirements and Best Practices

Pharmaguideline
7,078 回視聴 - 2 年前
10:35

FDA-NIH 2024 | D1S04 - Chemistry, Manufacturing and Controls: Regulatory Considerations and Resource

U.S. Food and Drug Administration
206 回視聴 - 1 か月前
40:34

eCTD Module 1: FDA, EMA, and Japan Requirements | ICH M4 Guidelines by Peivand Pirouzi, Ph.D

Crown College of Canada
303 回視聴 - 9 か月前
8:03

FDA Requirements for Electronic Source Data in Clinical Investigations

Kathy Barnett
55 回視聴 - 8 か月前
5:05

Regulatory Compliance : Meeting FDA Standards in Drug Manufacturing

Pharmaguideline
3,007 回視聴 - 11 か月前
1:28:37

FDA Cybersecurity and Software Policy Updates: Navigating the New FDA Guidance Documents for MedTech

MCRA, an IQVIA business
1,990 回視聴 - 2 年前
29:14

Developing and Maintaining an FDA Compliant Complaint Handling Process

Medmarc
245 回視聴 - 5 か月前
1:36:15

Software Validation Documentation for FDA 510(k) pre-market notification submission

Medical Device Academy
9,096 回視聴 - 5 年前
7:57

Complying with FDA Guidance Documents

MedTech Crossroads
307 回視聴 - 1 年前