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Search in Pharmaceuticals returned 45,007 results.

Implementing FDA's 21 CFR 111 for Dietary Supplements - Product Thumbnail Image

Implementing FDA's 21 CFR 111 for Dietary Supplements

  • Training
  • 75 Minutes
  • Global
Understanding the Current FDA Requirements for Raw Materials and Components - Product Thumbnail Image

Understanding the Current FDA Requirements for Raw Materials and Components

  • Training
  • 90 Minutes
  • Global
Do you understand the FDA Guidance "Recognition and Use of Consensus Standards"? - Product Thumbnail Image

Do you understand the FDA Guidance "Recognition and Use of Consensus Standards"?

  • Training
  • 60 Minutes
  • Global
Lean Approaches to Development of HPLC Methods for Drug Products - Product Thumbnail Image

Lean Approaches to Development of HPLC Methods for Drug Products

  • Training
  • 90 Minutes
  • Global
Qualification Sample Size and Statistical Confidence for Pharma Process Performance Qualification (PPQ) - Product Thumbnail Image

Qualification Sample Size and Statistical Confidence for Pharma Process Performance Qualification (PPQ)

  • Training
  • 90 Minutes
  • Global
Updated EU filing and registration procedures (including the new variation rules coming in to force) - Product Thumbnail Image

Updated EU filing and registration procedures (including the new variation rules coming in to force)

  • Training
  • 60 Minutes
  • Europe
Introduction of Post-Marketing Drug Safety Surveillance: Pharmacovigilance in FDA / CDER - Product Thumbnail Image

Introduction of Post-Marketing Drug Safety Surveillance: Pharmacovigilance in FDA / CDER

  • Training
  • 90 Minutes
  • Global
Ensuring Legally-Effective Informed Consent: Basic to Advanced Issues for Investigators and IRBs - Product Thumbnail Image

Ensuring Legally-Effective Informed Consent: Basic to Advanced Issues for Investigators and IRBs

  • Training
  • 90 Minutes
  • Global
Current Issues in the Regulation of Dietary Supplements - Product Thumbnail Image

Current Issues in the Regulation of Dietary Supplements

  • Training
  • 90 Minutes
  • Global
Changes in US FDA Enforcement - Product Thumbnail Image

Changes in US FDA Enforcement

  • Training
  • 90 Minutes
  • United States
Current Trends in FDA Inspections - Product Thumbnail Image

Current Trends in FDA Inspections

  • Training
  • 90 Minutes
  • Global
Site Preparation Strategy and Successful FDA Inspection - Product Thumbnail Image

Site Preparation Strategy and Successful FDA Inspection

  • Training
  • 60 Minutes
  • Global
Selecting the Most Appropriate Predicate Device(S) for your 510(k) Application - Product Thumbnail Image

Selecting the Most Appropriate Predicate Device(S) for your 510(k) Application

  • Training
  • 60 Minutes
  • Global
Equipment Requalification: What and When it is Really Required? - Product Thumbnail Image

Equipment Requalification: What and When it is Really Required?

  • Training
  • 60 Minutes
  • Global
Adverse Event Reporting Requirements for Dietary Supplements and OTC Drugs - Product Thumbnail Image

Adverse Event Reporting Requirements for Dietary Supplements and OTC Drugs

  • Training
  • 90 Minutes
  • Global
The New European Union Clinical Trials Regulation: An Analysis of the Key Changes and their Implications for Future Clinical Trials - Product Thumbnail Image

The New European Union Clinical Trials Regulation: An Analysis of the Key Changes and their Implications for Future Clinical Trials

  • Training
  • 60 Minutes
  • Europe
LDT including CDx; CLIA versus FDA's Authority - Product Thumbnail Image

LDT including CDx; CLIA versus FDA's Authority

  • Training
  • 60 Minutes
  • Global
How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA) - Product Thumbnail Image

How to respond to GXP (GCP, GLP, GMP, GPV) Inspection and Audit Findings using Correction and Preventative Action (CAPA)

  • Training
  • 60 Minutes
  • Global
Managing the Trial Master File - Considerations for Moving to Electronic TMFs - Product Thumbnail Image

Managing the Trial Master File - Considerations for Moving to Electronic TMFs

  • Training
  • 60 Minutes
  • Global
Are you prepared for a regulatory audit from FDA or any other regulatory body? - Product Thumbnail Image

Are you prepared for a regulatory audit from FDA or any other regulatory body?

  • Training
  • 90 Minutes
  • Global
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