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Search in Pharmaceuticals returned 45,007 results.

CDISC for US FDA Submissions - Are you Compliant? - Product Thumbnail Image

CDISC for US FDA Submissions - Are you Compliant?

  • Training
  • 90 Minutes
  • United States
Applying Quality Systems Concepts to Clinical Research Activities - Product Thumbnail Image

Applying Quality Systems Concepts to Clinical Research Activities

  • Training
  • 60 Minutes
  • Global
US FDA's Pre-Approval Inspection Program - Product Thumbnail Image

US FDA's Pre-Approval Inspection Program

  • Training
  • 60 Minutes
  • United States
How to Select a CRO; Best Practices - Product Thumbnail Image

How to Select a CRO; Best Practices

  • Training
  • 60 Minutes
  • Global
Investigator Initiated (Sponsored) Trials - ISSs - Product Thumbnail Image

Investigator Initiated (Sponsored) Trials - ISSs

  • Training
  • 60 Minutes
  • Global
Test Article Management and Characterization for Drugs and Devices - Product Thumbnail Image

Test Article Management and Characterization for Drugs and Devices

  • Training
  • 90 Minutes
  • Global
Biomarkers for Drug Development: The Emerging Regulatory Landscape - Product Thumbnail Image

Biomarkers for Drug Development: The Emerging Regulatory Landscape

  • Training
  • 60 Minutes
  • Global
How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices - Product Thumbnail Image

How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices

  • Training
  • 90 Minutes
  • Global
Making Sense of FDA's (proposed) Rules for the Development and Approval of Biosimilars - Product Thumbnail Image

Making Sense of FDA's (proposed) Rules for the Development and Approval of Biosimilars

  • Training
  • 60 Minutes
  • Global
Good Laboratory Practices for Bioanalytical Laboratories - Product Thumbnail Image

Good Laboratory Practices for Bioanalytical Laboratories

  • Training
  • 90 Minutes
  • Global
An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials - Product Thumbnail Image

An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials

  • Training
  • 90 Minutes
  • Global
Ethics and Scientific Misconduct in Regulated Studies - Product Thumbnail Image

Ethics and Scientific Misconduct in Regulated Studies

  • Training
  • 60 Minutes
  • Global
Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies - Product Thumbnail Image

Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies

  • Training
  • 60 Minutes
  • Global
Changes to Good Pharmacovigilance Practices in the EU - Product Thumbnail Image

Changes to Good Pharmacovigilance Practices in the EU

  • Training
  • 90 Minutes
  • Europe
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial - Product Thumbnail Image

Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial

  • Training
  • 90 Minutes
  • Global
Trial Master File for Research Sites: Can You Pass FDA Inspection? - Product Thumbnail Image

Trial Master File for Research Sites: Can You Pass FDA Inspection?

  • Training
  • 60 Minutes
  • Global
Recommendations for Cell Banks used in GXP testing - Product Thumbnail Image

Recommendations for Cell Banks used in GXP testing

  • Training
  • 60 Minutes
  • Global
Issue Detection and Escalation in Clinical Trial Settings - Product Thumbnail Image

Issue Detection and Escalation in Clinical Trial Settings

  • Training
  • 60 Minutes
  • Global
The U.S. FDA's New Global Engagement Initiative - Product Thumbnail Image

The U.S. FDA's New Global Engagement Initiative

  • Training
  • 90 Minutes
  • United States, Global United States, Global
REMS Update: Risk Evaluation and Mitigation Strategies - what do you need to do now? - Product Thumbnail Image

REMS Update: Risk Evaluation and Mitigation Strategies - what do you need to do now?

  • Training
  • 60 Minutes
  • Global
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