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Search in Pharmaceuticals returned 45,007 results.

21 CFR 111 GMP Dietary Supplement Laboratory - Product Thumbnail Image

21 CFR 111 GMP Dietary Supplement Laboratory

  • Training
  • 60 Minutes
  • Global
Good Deviation Practice: What You Need to Know - Product Thumbnail Image

Good Deviation Practice: What You Need to Know

  • Training
  • 60 Minutes
  • Global
Tools for Human Error Reduction - Product Thumbnail Image

Tools for Human Error Reduction

  • Training
  • 90 Minutes
  • Global
How to Survive FDA's New Inspection and Enforcement Practices - Product Thumbnail Image

How to Survive FDA's New Inspection and Enforcement Practices

  • Training
  • 75 Minutes
  • Global
Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance - Product Thumbnail Image

Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance

  • Training
  • 60 Minutes
  • Global
Making All Data Count: FDA Acceptance of non-US Clinical Trials - Product Thumbnail Image

Making All Data Count: FDA Acceptance of non-US Clinical Trials

  • Training
  • 90 Minutes
  • Global
The Sunshine Act Reporting for Clinical Trials - Product Thumbnail Image

The Sunshine Act Reporting for Clinical Trials

  • Training
  • 60 Minutes
  • Global
Creating a Global Regulatory Plan - Product Thumbnail Image

Creating a Global Regulatory Plan

  • Training
  • 60 Minutes
  • Global
Understanding FDA Regulations and Role in Opioid Pain Management - Product Thumbnail Image

Understanding FDA Regulations and Role in Opioid Pain Management

  • Training
  • 60 Minutes
  • Global
How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices - Product Thumbnail Image

How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices

  • Training
  • 60 Minutes
  • Global
Good Documentation Practices (GDP) - Product Thumbnail Image

Good Documentation Practices (GDP)

  • Training
  • 60 Minutes
  • Global
Corrective and Preventive Action Utilizing the Principles of Lean Documents and Lean Configuration - Product Thumbnail Image

Corrective and Preventive Action Utilizing the Principles of Lean Documents and Lean Configuration

  • Training
  • 90 Minutes
  • Global
Thorough and Complete Investigations and Follow-Up - A Current Regulatory Expectation - Product Thumbnail Image

Thorough and Complete Investigations and Follow-Up - A Current Regulatory Expectation

  • Training
  • 90 Minutes
  • Global
Fraud in Clinical Research - Product Thumbnail Image

Fraud in Clinical Research

  • Training
  • 60 Minutes
  • Global
FDA vs. EU Inspections - Getting Prepared and What are Differences - Product Thumbnail Image

FDA vs. EU Inspections - Getting Prepared and What are Differences

  • Training
  • 75 Minutes
  • Europe
Clinical Trial Liability Lawsuits - Product Thumbnail Image

Clinical Trial Liability Lawsuits

  • Training
  • 60 Minutes
  • Global
ICH Q10 - Moving From GMPs To A Pharmaceutical Quality System - Product Thumbnail Image

ICH Q10 - Moving From GMPs To A Pharmaceutical Quality System

  • Training
  • 90 Minutes
  • Global
A Unified Approach to Complaints, Servicing, and FDA Reporting - Product Thumbnail Image

A Unified Approach to Complaints, Servicing, and FDA Reporting

  • Training
  • 90 Minutes
  • Global
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials - Product Thumbnail Image

Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials

  • Training
  • 90 Minutes
  • Global
Major Changes to Clinical Trials in Europe - The New EU Clinical Trials Regulation - What Can We Expect for Compliance? - Product Thumbnail Image

Major Changes to Clinical Trials in Europe - The New EU Clinical Trials Regulation - What Can We Expect for Compliance?

  • Training
  • 60 Minutes
  • Europe
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