+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Search in Pharmaceuticals returned 45,007 results.

Meeting FDA Requirements for Over-the-Counter / OTC Drug Labeling - Product Thumbnail Image

Meeting FDA Requirements for Over-the-Counter / OTC Drug Labeling

  • Training
  • 60 Minutes
  • Global
Delivering Biopharmaceutical Facilities in a Risk Based World: The Role of GEP, QbD, and E2500 - Product Thumbnail Image

Delivering Biopharmaceutical Facilities in a Risk Based World: The Role of GEP, QbD, and E2500

  • Training
  • 60 Minutes
  • Global
Combination products and convergence: an overview of clinical benefits, regulatory issues and manufacturing challenges - part 1 - Product Thumbnail Image

Combination products and convergence: an overview of clinical benefits, regulatory issues and manufacturing challenges - part 1

  • Training
  • 90 Minutes
  • Global
Risk Evaluation and Mitigation Strategies (REMS) what you need to know in order to comply with FDA's new requirements - Product Thumbnail Image

Risk Evaluation and Mitigation Strategies (REMS) what you need to know in order to comply with FDA's new requirements

  • Training
  • 60 Minutes
  • Global
21 CFR Part 11 compliance under the Obama administration - Product Thumbnail Image

21 CFR Part 11 compliance under the Obama administration

  • Training
  • 60 Minutes
  • Global
cGMP 'Pitfalls' in the QC Laboratory-Preparing the QC Laboratory and Staff for an FDA Inspection - Product Thumbnail Image

cGMP 'Pitfalls' in the QC Laboratory-Preparing the QC Laboratory and Staff for an FDA Inspection

  • Training
  • 60 Minutes
  • Global
Surprise FDA GMP inspection - how to prepare for it - Product Thumbnail Image

Surprise FDA GMP inspection - how to prepare for it

  • Training
  • 90 Minutes
  • Global
Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies - Product Thumbnail Image

Using ICH Q9 and Recent FDA Comments as the Foundation for the Planning, Development and Execution of Risk-Based Cleaning Validation Studies

  • Training
  • 90 Minutes
  • Global
Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter - Product Thumbnail Image

Residual Solvent Analysis According to USP <467> - Understanding and implementing the new USP chapter

  • Training
  • 60 Minutes
  • Global
Design History Files and Technical Files under US FDA and EU MDD - Product Thumbnail Image

Design History Files and Technical Files under US FDA and EU MDD

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies - Product Thumbnail Image

Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies

  • Training
  • Global
Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices - Product Thumbnail Image

Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices

  • Training
  • 90 Minutes
  • Global
Clearing up Roles and Responsibilities in the GLPs - Product Thumbnail Image

Clearing up Roles and Responsibilities in the GLPs

  • Training
  • 60 Minutes
  • Global
Gage R & R - Improving the Reliability and Reducing the Variation of Your Measurement System - Product Thumbnail Image

Gage R & R - Improving the Reliability and Reducing the Variation of Your Measurement System

  • Training
  • 60 Minutes
  • Global
Principal Investigator responsibility in Research Involving Human Subjects: The International Conference on Harmonization (ICH) view - Product Thumbnail Image

Principal Investigator responsibility in Research Involving Human Subjects: The International Conference on Harmonization (ICH) view

  • Training
  • 90 Minutes
  • Global
510(k) Applications made Simple - Product Thumbnail Image

510(k) Applications made Simple

  • Training
  • 60 Minutes
  • Global
Clinical Trials Process: Study Sponsor's and Investigator's Responsibilities - Product Thumbnail Image

Clinical Trials Process: Study Sponsor's and Investigator's Responsibilities

  • Training
  • 60 Minutes
  • Global
Best Practices in GLP Final Reporting and Study Closure - Product Thumbnail Image

Best Practices in GLP Final Reporting and Study Closure

  • Training
  • 60 Minutes
  • Global
FDA at the Door: Ten Essential Steps for Inspection Success - Product Thumbnail Image

FDA at the Door: Ten Essential Steps for Inspection Success

  • Training
  • 60 Minutes
  • Global
Quality Expectations for Drugs and Biologics during Early Development: Phase 3 and NDA - Product Thumbnail Image

Quality Expectations for Drugs and Biologics during Early Development: Phase 3 and NDA

  • Training
  • 75 Minutes
  • Global
Loading Indicator