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Search in Pharmaceuticals returned 45,007 results.

Major Changes to the EU Clinical Trials Regulation: What is Required for Compliance - Product Thumbnail Image

Major Changes to the EU Clinical Trials Regulation: What is Required for Compliance

  • Training
  • 60 Minutes
  • Europe
Regulatory Documentation for Clinical Trials - Product Thumbnail Image

Regulatory Documentation for Clinical Trials

  • Training
  • 60 Minutes
  • Global
How To Translate Academic and Discovery Assays Into GLP Compliant Assays - Product Thumbnail Image

How To Translate Academic and Discovery Assays Into GLP Compliant Assays

  • Training
  • 60 Minutes
  • Global
Pharmaceutical Government Price Reporting: Impact of Obamacare - Product Thumbnail Image

Pharmaceutical Government Price Reporting: Impact of Obamacare

  • Training
  • 60 Minutes
  • Global
Archiving Clinical Trial Documents - Understanding Regulatory Requirements for Paper and Electronic Records - Product Thumbnail Image

Archiving Clinical Trial Documents - Understanding Regulatory Requirements for Paper and Electronic Records

  • Training
  • 60 Minutes
  • Global
Marketing Beverages, Fruit Juice and Sports Drinks in Compliance with FDA Regulations - Product Thumbnail Image

Marketing Beverages, Fruit Juice and Sports Drinks in Compliance with FDA Regulations

  • Training
  • 60 Minutes
  • Global
Quality Control for Microbiological Media and Reagents - Product Thumbnail Image

Quality Control for Microbiological Media and Reagents

  • Training
  • 60 Minutes
  • Global
Drug Master Files: New Requirements under GDUFA - Product Thumbnail Image

Drug Master Files: New Requirements under GDUFA

  • Training
  • 60 Minutes
  • Global
Walking the Minefield of Clinical Trial Budgets and Contracts; A Primer for Research Managers - Product Thumbnail Image

Walking the Minefield of Clinical Trial Budgets and Contracts; A Primer for Research Managers

  • Training
  • 90 Minutes
  • Global
How to Withstand an FDA Audit of your Facility - Product Thumbnail Image

How to Withstand an FDA Audit of your Facility

  • Training
  • 60 Minutes
  • Global
Verification of Compendial Methods According to the Revised USP Chapter <1226> - Product Thumbnail Image

Verification of Compendial Methods According to the Revised USP Chapter <1226>

  • Training
  • 75 Minutes
  • Global
Facility Operations, Maintenance, and Calibration - Product Thumbnail Image

Facility Operations, Maintenance, and Calibration

  • Training
  • 90 Minutes
  • Global
Process Validation for Medical Device Manufacturers - Product Thumbnail Image

Process Validation for Medical Device Manufacturers

  • Training
  • 90 Minutes
  • Global
Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall - Product Thumbnail Image

Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall

  • Training
  • 60 Minutes
  • Global
Equipment Calibration in FDA QSR - Regulations and Warning Letters - Product Thumbnail Image

Equipment Calibration in FDA QSR - Regulations and Warning Letters

  • Training
  • 90 Minutes
  • Global
FDA Enforcement and Your Compliance Program - Product Thumbnail Image

FDA Enforcement and Your Compliance Program

  • Training
  • 60 Minutes
  • Global
Essential Last Minute Preparation for an Imminent FDA Inspection - Product Thumbnail Image

Essential Last Minute Preparation for an Imminent FDA Inspection

  • Training
  • 60 Minutes
  • Global
Dietary Supplements Ingredient and Labeling Compliance - Product Thumbnail Image

Dietary Supplements Ingredient and Labeling Compliance

  • Training
  • 60 Minutes
  • Global
FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations - Product Thumbnail Image

FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations

  • Training
  • 90 Minutes
  • Global
FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance - Product Thumbnail Image

FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance

  • Training
  • 70 Minutes
  • Global
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