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Search in Pharmaceuticals returned 45,007 results.

When Studies are Exempted from IND Requirements: Understanding the Criteria and the Consequences - Product Thumbnail Image

When Studies are Exempted from IND Requirements: Understanding the Criteria and the Consequences

  • Training
  • 60 Minutes
  • Global
Recruitment and Informed Consent: The Cornerstone of Ethical Clinical Research - Product Thumbnail Image

Recruitment and Informed Consent: The Cornerstone of Ethical Clinical Research

  • Training
  • 60 Minutes
  • Global
Good Laboratory Practices for Food Manufacturing - Product Thumbnail Image

Good Laboratory Practices for Food Manufacturing

  • Training
  • 90 Minutes
  • Global
Biomarkers in Drug Development - Product Thumbnail Image

Biomarkers in Drug Development

  • Training
  • 60 Minutes
  • Global
Pre-Market Submission Implications of FDA's Human Factors Guidance and Device Priority List - Product Thumbnail Image

Pre-Market Submission Implications of FDA's Human Factors Guidance and Device Priority List

  • Training
  • 90 Minutes
  • Global
Biological Facility Design: Design for Compliance - Product Thumbnail Image

Biological Facility Design: Design for Compliance

  • Training
  • 60 Minutes
  • Global
GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry - Product Thumbnail Image

GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry

  • Training
  • 90 Minutes
  • Global
FDA Inspection Preparedness - Product Thumbnail Image

FDA Inspection Preparedness

  • Training
  • 60 Minutes
  • Global
FDA's New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices - Product Thumbnail Image

FDA's New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices

  • Training
  • 90 Minutes
  • Global
New Part 11 Guidance for Clinical Trials: What This Means for You - Product Thumbnail Image

New Part 11 Guidance for Clinical Trials: What This Means for You

  • Training
  • 60 Minutes
  • Global
Process Robustness: The New FDA Paradigm - Product Thumbnail Image

Process Robustness: The New FDA Paradigm

  • Training
  • 90 Minutes
  • Global
How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment - Product Thumbnail Image

How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment

  • Training
  • 60 Minutes
  • Global
Introduction to the FDA and Your First FDA Meeting - Product Thumbnail Image

Introduction to the FDA and Your First FDA Meeting

  • Training
  • 60 Minutes
  • Global
Upcoming Changes to ISO 14-644 Parts 1 and 2 - Cleanrooms and Associated Controlled Environments - Product Thumbnail Image

Upcoming Changes to ISO 14-644 Parts 1 and 2 - Cleanrooms and Associated Controlled Environments

  • Training
  • 60 Minutes
  • Global
FDA's new enforcement initiative - Strategic Software Validation Planning for Executives and Managers - Product Thumbnail Image

FDA's new enforcement initiative - Strategic Software Validation Planning for Executives and Managers

  • Training
  • 60 Minutes
  • Global
Medical Foods: Practical Tips to Meet FDA Requirements for Claims and Quality - Product Thumbnail Image

Medical Foods: Practical Tips to Meet FDA Requirements for Claims and Quality

  • Training
  • 60 Minutes
  • Global
How's your HACCP? Developing a HACCP program that is effective, appropriate and compliant - Product Thumbnail Image

How's your HACCP? Developing a HACCP program that is effective, appropriate and compliant

  • Training
  • 75 Minutes
  • Global
FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Product Thumbnail Image

FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes

  • Training
  • 60 Minutes
  • Global
Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs) - Product Thumbnail Image

Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs)

  • Training
  • 90 Minutes
  • Global
Acceptance Activities in FDA QSR - Product Thumbnail Image

Acceptance Activities in FDA QSR

  • Training
  • 90 Minutes
  • Global
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