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Search in Pharmaceuticals returned 45,007 results.

How to Transition from Paper to Electronic Records in a Regulatory Environment - Product Thumbnail Image

How to Transition from Paper to Electronic Records in a Regulatory Environment

  • Training
  • 75 Minutes
  • Global
Laboratory Investigations for Out of Specification Results - Product Thumbnail Image

Laboratory Investigations for Out of Specification Results

  • Training
  • 90 Minutes
  • Global
Does your QC lab do GMP and non-GMP activities? - Product Thumbnail Image

Does your QC lab do GMP and non-GMP activities?

  • Training
  • 60 Minutes
  • Global
Change Control Best Practices: Avoiding Unintended Consequences of Changes - Product Thumbnail Image

Change Control Best Practices: Avoiding Unintended Consequences of Changes

  • Training
  • 90 Minutes
  • Global
Understanding and Preparing for FDA Pharmaceutical Inspections (Recorded) - Product Thumbnail Image

Understanding and Preparing for FDA Pharmaceutical Inspections (Recorded)

  • Training
  • June 2024
  • 90 Minutes
  • Global
The eSTAR Submission Program for 510(k)s, IDEs, De Novos, PMAs, and Q-Submissions - Product Thumbnail Image

The eSTAR Submission Program for 510(k)s, IDEs, De Novos, PMAs, and Q-Submissions

  • Training
  • 90 Minutes
  • Global
Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3 - Product Thumbnail Image

Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3

  • Training
  • 90 Minutes
  • Global
The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs - Product Thumbnail Image

The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs

  • Training
  • 90 Minutes
  • United States
Drug Labeling and Packaging: Meeting Regulatory Requirements - Product Thumbnail Image

Drug Labeling and Packaging: Meeting Regulatory Requirements

  • Training
  • 60 Minutes
  • Global
US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes - Product Thumbnail Image

US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes

  • Training
  • 90 Minutes
  • United States
Design History File (DHF) Remediation using Principles of Lean Documents and Lean Configuration - Product Thumbnail Image

Design History File (DHF) Remediation using Principles of Lean Documents and Lean Configuration

  • Training
  • 90 Minutes
  • Global
How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity - Product Thumbnail Image

How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity

  • Training
  • 90 Minutes
  • Global
EU's New Regulation 536/2014 on Clinical Trials - Product Thumbnail Image

EU's New Regulation 536/2014 on Clinical Trials

  • Training
  • 90 Minutes
  • Europe
Predicting Product Life Using Reliability Analysis Methods - Product Thumbnail Image

Predicting Product Life Using Reliability Analysis Methods

  • Training
  • 90 Minutes
  • Global
Good Documentation Practice (GDP) and FDA Validation Compliance for Regulated Computer Systems and Data - Product Thumbnail Image

Good Documentation Practice (GDP) and FDA Validation Compliance for Regulated Computer Systems and Data

  • Training
  • 90 Minutes
  • Global
Risk Management of Raw Materials in a GMP Environment - Product Thumbnail Image

Risk Management of Raw Materials in a GMP Environment

  • Training
  • 90 Minutes
  • Global
The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process - Product Thumbnail Image

The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process

  • Training
  • 90 Minutes
  • Global
Conducting Effective Mock FDA Inspections - Product Thumbnail Image

Conducting Effective Mock FDA Inspections

  • Training
  • 90 Minutes
  • Global
Normality Testing: Applications and Issues - Product Thumbnail Image

Normality Testing: Applications and Issues

  • Training
  • 90 Minutes
  • Global
USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms - Product Thumbnail Image

USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms

  • Training
  • 90 Minutes
  • Global
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