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Search in Pharmaceuticals returned 45,007 results.

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
Technology Transfer of a Pharmaceutical Manufacturing Process - Product Thumbnail Image

Technology Transfer of a Pharmaceutical Manufacturing Process

  • Training
  • 90 Minutes
  • Global
Pediatric Drug Development - Relevant FDA Laws and Changing Approach - Product Thumbnail Image

Pediatric Drug Development - Relevant FDA Laws and Changing Approach

  • Training
  • 60 Minutes
  • Global
Cleaning Validation Swab Recovery Studies and Analysis - Product Thumbnail Image

Cleaning Validation Swab Recovery Studies and Analysis

  • Training
  • 60 Minutes
  • Global
Simplifying the Dietary Supplement cGMPs for Those Confused by the Regulations - Product Thumbnail Image

Simplifying the Dietary Supplement cGMPs for Those Confused by the Regulations

  • Training
  • 60 Minutes
  • Global
Understanding CFR Part 210-211 Requirements for Drug Products - Product Thumbnail Image

Understanding CFR Part 210-211 Requirements for Drug Products

  • Training
  • 90 Minutes
  • Global
The 510(k) Process and Risk Management - Product Thumbnail Image

The 510(k) Process and Risk Management

  • Training
  • 90 Minutes
  • Global
Internal Auditing in Pharmaceutical Manufacturing - Lightning Rod & Steam Valve - Product Thumbnail Image

Internal Auditing in Pharmaceutical Manufacturing - Lightning Rod & Steam Valve

  • Training
  • 60 Minutes
  • Global
Responding to Unsolicited Requests for Off-Label Information - Product Thumbnail Image

Responding to Unsolicited Requests for Off-Label Information

  • Training
  • 90 Minutes
  • Global
FDA Regulation of Therapeutic Use of Live Cells - Product Thumbnail Image

FDA Regulation of Therapeutic Use of Live Cells

  • Training
  • 60 Minutes
  • Global
CFR 21 Part 11 and Annex 11: How to Avoid the Audit Traps - Product Thumbnail Image

CFR 21 Part 11 and Annex 11: How to Avoid the Audit Traps

  • Training
  • 75 Minutes
  • Global
Overview of Importing Foreign Cosmetic and OTC Products - Product Thumbnail Image

Overview of Importing Foreign Cosmetic and OTC Products

  • Training
  • 60 Minutes
  • Global
Regulatory Compliance for Food Supplements in the EU - Registration, Labeling, Acceptable Marketing Claims - Product Thumbnail Image

Regulatory Compliance for Food Supplements in the EU - Registration, Labeling, Acceptable Marketing Claims

  • Training
  • 90 Minutes
  • Europe
FDA Regulatory Actions: It's Not Just about Warning Letters - Product Thumbnail Image

FDA Regulatory Actions: It's Not Just about Warning Letters

  • Training
  • 60 Minutes
  • Global
Essential Do's and Don'ts for Navigating a Successful 505(b)(2) Drug Application - Product Thumbnail Image

Essential Do's and Don'ts for Navigating a Successful 505(b)(2) Drug Application

  • Training
  • 60 Minutes
  • Global
Understanding and Interpreting the EMA Reflection Paper on GCP Compliance in Relation to Trial Master Files (paper and/or electronic) for Management, Audit and Inspection of Clinical Trials - Product Thumbnail Image

Understanding and Interpreting the EMA Reflection Paper on GCP Compliance in Relation to Trial Master Files (paper and/or electronic) for Management, Audit and Inspection of Clinical Trials

  • Training
  • 60 Minutes
  • Global
FDA Software Validation Self-Check - plan an effective Internal Audit program - Product Thumbnail Image

FDA Software Validation Self-Check - plan an effective Internal Audit program

  • Training
  • 60 Minutes
  • Global
FDA Warning Letter Closeout Program - Product Thumbnail Image

FDA Warning Letter Closeout Program

  • Training
  • 60 Minutes
  • Global
An Introduction to FDA's Regulation of Over-the-Counter (OTC) Drug Products - Product Thumbnail Image

An Introduction to FDA's Regulation of Over-the-Counter (OTC) Drug Products

  • Training
  • 90 Minutes
  • Global
Medical Foods: Understanding what Constitutes a Medical Food for FDA Regulatory Purposes and Strategies for Successfully Commercializing such Products in the U.S. - Product Thumbnail Image

Medical Foods: Understanding what Constitutes a Medical Food for FDA Regulatory Purposes and Strategies for Successfully Commercializing such Products in the U.S.

  • Training
  • 90 Minutes
  • United States
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