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Search in Pharmaceuticals returned 45,007 results.

21 CFR Part 11 compliance for Electronic Medical Records - Product Thumbnail Image

21 CFR Part 11 compliance for Electronic Medical Records

  • Training
  • 60 Minutes
  • Global
Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance - Product Thumbnail Image

Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance

  • Training
  • 75 Minutes
  • Europe
Best Practices for Maintaining an IND and IDE Application with FDA - Product Thumbnail Image

Best Practices for Maintaining an IND and IDE Application with FDA

  • Training
  • 60 Minutes
  • Global
Life Cycle Validation of GMP Potency Bioassays - Product Thumbnail Image

Life Cycle Validation of GMP Potency Bioassays

  • Training
  • 90 Minutes
  • Global
Good Documentation Practices for GXPs - Product Thumbnail Image

Good Documentation Practices for GXPs

  • Training
  • 60 Minutes
  • Global
FDA's Rules for Financial Disclosure in Clinical Trials Clarified: New Guidance, Practical Application - Product Thumbnail Image

FDA's Rules for Financial Disclosure in Clinical Trials Clarified: New Guidance, Practical Application

  • Training
  • 60 Minutes
  • Global
Managing Immunogenicity Risk in Biopharmaceuticals - Product Thumbnail Image

Managing Immunogenicity Risk in Biopharmaceuticals

  • Training
  • 60 Minutes
  • Global
Accelerating Bioassay Transfer in a GMP Environment - Product Thumbnail Image

Accelerating Bioassay Transfer in a GMP Environment

  • Training
  • 60 Minutes
  • Global
The 510(k) Process: Evaluating Substantial Equivalence in Premarket Notifications - Product Thumbnail Image

The 510(k) Process: Evaluating Substantial Equivalence in Premarket Notifications

  • Training
  • 60 Minutes
  • Global
Validation of HPLC/UPLC Methodologies - Product Thumbnail Image

Validation of HPLC/UPLC Methodologies

  • Training
  • 60 Minutes
  • Global
Analytical Method Validation Under Good Laboratory Practices (GLPs) - Product Thumbnail Image

Analytical Method Validation Under Good Laboratory Practices (GLPs)

  • Training
  • 60 Minutes
  • Global
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results - Product Thumbnail Image

Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results

  • Training
  • 120 Minutes
  • Global
QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer - Product Thumbnail Image

QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer

  • Training
  • 90 Minutes
  • Global
FDA Compliance and Clinical Trial Computer System Validation - Product Thumbnail Image

FDA Compliance and Clinical Trial Computer System Validation

  • Training
  • 60 Minutes
  • Global
Extractables and Leachables in Early Phase Development - Product Thumbnail Image

Extractables and Leachables in Early Phase Development

  • Training
  • 60 Minutes
  • Global
Creating Powerful PowerPoint Decks - Product Thumbnail Image

Creating Powerful PowerPoint Decks

  • Training
  • 90 Minutes
  • Global
Creating Effective SOPs for Regulatory Compliance - Product Thumbnail Image

Creating Effective SOPs for Regulatory Compliance

  • Training
  • 60 Minutes
  • Global
Effective Annual U.S. FDA CGMP Training - Product Thumbnail Image

Effective Annual U.S. FDA CGMP Training

  • Training
  • 60 Minutes
  • United States
FSMA Gives FDA Fee Collection Authority for Certain Violations - Product Thumbnail Image

FSMA Gives FDA Fee Collection Authority for Certain Violations

  • Training
  • 90 Minutes
  • Global
Creating FDA-compliant cGMP Training Program - Product Thumbnail Image

Creating FDA-compliant cGMP Training Program

  • Training
  • 60 Minutes
  • Global
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