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Search in Pharmaceuticals returned 45,096 results.

How To Implement An Effective Human Error Reduction Program - Product Thumbnail Image

How To Implement An Effective Human Error Reduction Program

  • Training
  • 90 Minutes
  • Global
FDA Establishment Inspections - What to Expect? - Product Thumbnail Image

FDA Establishment Inspections - What to Expect?

  • Training
  • 60 Minutes
  • Global
Combination Drug/Device Products CGMPs - Final Rule - Product Thumbnail Image

Combination Drug/Device Products CGMPs - Final Rule

  • Training
  • 90 Minutes
  • Global
Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process Activities - Product Thumbnail Image

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process Activities

  • Training
  • 90 Minutes
  • Global
Handling OOS Test Results and Completing Robust Investigations - Product Thumbnail Image

Handling OOS Test Results and Completing Robust Investigations

  • Training
  • 90 Minutes
  • Global
Management of the Data Safety Management Committee for Clinical Trials - Product Thumbnail Image

Management of the Data Safety Management Committee for Clinical Trials

  • Training
  • 60 Minutes
  • Global
Consents and 42 CFR Part 2 - New Rules for Re-Release of Substance Use Disorder Information - Product Thumbnail Image

Consents and 42 CFR Part 2 - New Rules for Re-Release of Substance Use Disorder Information

  • Training
  • 90 Minutes
  • Global
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists - Product Thumbnail Image

How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists

  • Training
  • 90 Minutes
  • Global
Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes - Product Thumbnail Image

Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes

  • Training
  • 90 Minutes
  • Global
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System - Product Thumbnail Image

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

  • Training
  • 90 Minutes
  • United States
How to Manage Your Vendors in Clinical Research - Product Thumbnail Image

How to Manage Your Vendors in Clinical Research

  • Training
  • 90 Minutes
  • Global
Use of Wearable Devices in Clinical Trials - Product Thumbnail Image

Use of Wearable Devices in Clinical Trials

  • Training
  • 60 Minutes
  • Global
How to Survive a DEA Inspection Series: For DEA Registered Analytical Labs and Research Facilities - Product Thumbnail Image

How to Survive a DEA Inspection Series: For DEA Registered Analytical Labs and Research Facilities

  • Training
  • 90 Minutes
  • Global
Pharmaceutical Water System: Design, Testing and Data Management - Product Thumbnail Image

Pharmaceutical Water System: Design, Testing and Data Management

  • Training
  • 90 Minutes
  • Global
Validation and Use of Excel® Spreadsheets in FDA Regulated Environments - Product Thumbnail Image

Validation and Use of Excel® Spreadsheets in FDA Regulated Environments

  • Training
  • 75 Minutes
  • Global
How to Survive a DEA Inspection Series - For Manufacturers of Controlled Substances - Product Thumbnail Image

How to Survive a DEA Inspection Series - For Manufacturers of Controlled Substances

  • Training
  • 90 Minutes
  • Global
Analytical Method Validation and Transfer - Product Thumbnail Image

Analytical Method Validation and Transfer

  • Training
  • 90 Minutes
  • Global
Aseptic Processing Overview and Validation - Product Thumbnail Image

Aseptic Processing Overview and Validation

  • Training
  • 90 Minutes
  • Global
Regulatory Inspections - How to prepare for a visit from an FDA Auditor - Product Thumbnail Image

Regulatory Inspections - How to prepare for a visit from an FDA Auditor

  • Training
  • 60 Minutes
  • Global
Implementation and Management of GMP Data Integrity - Product Thumbnail Image

Implementation and Management of GMP Data Integrity

  • Training
  • 90 Minutes
  • Global
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