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Search in Pharmaceuticals returned 45,007 results.

Effective Method Transfer of Complex Bioassays - Product Thumbnail Image

Effective Method Transfer of Complex Bioassays

  • Training
  • 60 Minutes
  • Global
The latest approach for complying with 21 CFR Part 11 - Product Thumbnail Image

The latest approach for complying with 21 CFR Part 11

  • Training
  • 60 Minutes
  • Global
Quality Planning Process and Procedure - Product Thumbnail Image

Quality Planning Process and Procedure

  • Training
  • 60 Minutes
  • Global
Validation of Potency Bioassays for Biologicals - Product Thumbnail Image

Validation of Potency Bioassays for Biologicals

  • Training
  • 60 Minutes
  • Global
FDA's cGMPs for the 21st Century Initiative - Product Thumbnail Image

FDA's cGMPs for the 21st Century Initiative

  • Training
  • Global
Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Risk Management - Product Thumbnail Image

Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Risk Management

  • Training
  • 60 Minutes
  • Global
Introduction to statistical Design and Analysis of Experiments (DOE) - Product Thumbnail Image

Introduction to statistical Design and Analysis of Experiments (DOE)

  • Training
  • 60 Minutes
  • Global
Designing Regulatory - Compliant Clinical Research Data Management Systems - Product Thumbnail Image

Designing Regulatory - Compliant Clinical Research Data Management Systems

  • Training
  • 60 Minutes
  • Global
Design Controls: What to know when it comes to FDA regulated industry? - Product Thumbnail Image

Design Controls: What to know when it comes to FDA regulated industry?

  • Training
  • 120 Minutes
  • Global
3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada - Product Thumbnail Image

3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

  • Training
  • 3 Hours
  • Europe, United States, ... Europe, United States, Canada
Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results - Product Thumbnail Image

Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results

  • Training
  • 120 Minutes
  • Global
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
Design Controls Basics - From Design Inputs to Design Outputs and Effective Design Transfer - Product Thumbnail Image

Design Controls Basics - From Design Inputs to Design Outputs and Effective Design Transfer

  • Training
  • 60 Minutes
  • Global
Viral Validation for Biopharmaceuticals - Product Thumbnail Image

Viral Validation for Biopharmaceuticals

  • Training
  • 60 Minutes
  • Global
Experiences of managing a quality management system for a virtual pharmaceutical company - Product Thumbnail Image

Experiences of managing a quality management system for a virtual pharmaceutical company

  • Training
  • 60 Minutes
  • Global
Designing Viral Clearance Studies for Biopharmaceuticals - Product Thumbnail Image

Designing Viral Clearance Studies for Biopharmaceuticals

  • Training
  • 90 Minutes
  • Global
Design Input: How to write requirements and modularize a product - Product Thumbnail Image

Design Input: How to write requirements and modularize a product

  • Training
  • 60 Minutes
  • Global
FDA Compliance and Quality inspections - Product Thumbnail Image

FDA Compliance and Quality inspections

  • Training
  • 60 Minutes
  • Global
Using the FDA guidance General Principles of Software Validation to strengthen your firm's software FDA compliance - Product Thumbnail Image

Using the FDA guidance General Principles of Software Validation to strengthen your firm's software FDA compliance

  • Training
  • Global
Making FMEA a More Efficient and Powerful Patient Safety Improvement Tool - Product Thumbnail Image

Making FMEA a More Efficient and Powerful Patient Safety Improvement Tool

  • Training
  • 60 Minutes
  • Global
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