fda compliance

Importing FDA-Regulated Products: The Import Process

10:55

Understanding FDA Inspections and Data

1:56:15

FDA Inspection and Compliance : Regulatory Requirements and Best Practices

6:05

New U.S. FDA Food Labeling Rules

2:37

FDA Inspection Readiness Training - Updated for 2022 - Brought to you by Compliance Architects LLC

1:25:46

ClinicalTrials.gov: Part 3 - CDER’s Compliance and Enforcement Activities

16:32

CDER BIMO GCP Compliance and Enforcement

2:25:17

FDA Commercial Tobacco Retail Compliance Check Inspection Program

6:14

FDA GMP Training

48:06

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

1:31:06

U.S. FDA Regulations for Dietary Supplements

55:51

What is FDA DSCSA compliance?

00:41

U.S. FDA Preventive Controls Requirements

1:01:23

What is FDA’s role in regulating drugs?

2:28

DSCSA 2023 Extension: Requirements and Compliance Guidelines #fda

00:42

FDA Drug Manufacturing Inspections - REdI 2020

52:33

FDA's New Food Safety Law

3:47

Tobacco Product Compliance Webinar: Updates for Importers

15:41

FDA 483 inspection

23:34

FDA Product Regulations Part 1 of 7

28:23

FDA 101 for Medical Devices

57:47

U.S. FDA Drug Labeling Requirements

49:43

Registrar Corp's FDA Compliance Monitor: Automate FSMA Compliance

1:45

Navigating FDA Regulations for Dietary Supplements

47:33

FDA Unique Device Identifier (UDI) Requirements

2:36

Preparing for an FDA inspection

7:13

Top 22 Tips for Writing for FDA Compliance

23:40

ClinicalTrials.gov: Part 1 - Meeting Transparency and Reporting Requirements

12:18

Regulatory Approaches to Dietary Supplements and their Claims

38:27

Reporting Individual Case Study Reports (ICSRs) to FAERS Using ICH E2B R3 Standards

1:04:56

FDA Tobacco Compliance Webinars: Importing Tobacco Products: Updates for Importers

13:53

What Is FDA Compliance? - Whiteboard Wednesday

2:44

ClinicalTrials.gov: Part 2 - Definitions, Laws, and Regulations

15:33

New U.S. FDA Food Labeling Rules

1:00:14

FDA Tobacco Compliance Webinars: Tobacco Product Listing Updates

7:08

Employees are the FIRST Line of Food Defense (English)

11:36

Regulatory compliance in clinical trials

4:33

21 cfr 210 211

30:06

Why Does The FDA Exist?

4:11

FDA UDI Regulation’s Impact on Medical Device Labelers Webinar

35:16

Supplier Evaluation & Assessment How to Meet FDA QSR & ISO 13485 Requirements

1:07:19

Ensuring FDA Compliance The Essential Guide to FDA 21CFR Part 11

38:03

FDA Compliance Monitor - Automate Supply Chain Risk Management

2:21

FDA Warning Letter

21:47

21 CFR, Parts 210 and 211

1:12:03

FDA Regulatory Education for Industry (REdI) Annual Conference 2023 – Plenary + Drugs Day 1

7:42:41

FDA Clinical Investigator Training Course (CITC) 2022, Day 1 – Part 3

1:10:23

21 CFR Part 11 Compliance for Excel Spreadsheets

1:51:00

21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar

11:00

FDA Fish and Fishery Products and Hazards Controls Guidance, 4th Edition: Introduction and Overview

34:44

Mastering FDA Inspections: Expert Tips for Effective Planning and Preparation

4:43

The Rulemaking Process: A Primer by FDA

1:57

FDA Registration and Listing Compliance Program (6/7) Drug Registration and Listing 2018

1:00:19

21CFR Part 58 - The Good Laboratory Practices (GLP) Regulation

11:01

Analyzing the FDA Process Validation Guidance

3:29

FDA Regulations and Medical Device Pathways to Market

28:21

FDA Inspections Part 1

12:02

Medical Device Regulations / FDA Approval

9:28

Compliance Insight FDA Consulting

42:27

Compliance Program and Case Study (7of8) Registration and Listing - Oct. 22, 2019

58:14