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Search in Pharmaceuticals returned 45,007 results.

Process Validation, planning, strategy, requirements, risk assessment, design description - Product Thumbnail Image

Process Validation, planning, strategy, requirements, risk assessment, design description

  • Training
  • 60 Minutes
  • Global
Pharmacovigilance aspects of licensing agreements - Product Thumbnail Image

Pharmacovigilance aspects of licensing agreements

  • Training
  • 60 Minutes
  • Global
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements - Product Thumbnail Image

Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements

  • Training
  • 75 Minutes
  • Global
Pharmaceutical Cleaning Validation - Product Thumbnail Image

Pharmaceutical Cleaning Validation

  • Training
  • 60 Minutes
  • Global
Differences in GMP Requirements between Drugs and Biologicals - Product Thumbnail Image

Differences in GMP Requirements between Drugs and Biologicals

  • Training
  • 60 Minutes
  • Global
Quality by Design: what the FDA wants, what you must do, how you can deliver to their expectations and what relief you can expect - Product Thumbnail Image

Quality by Design: what the FDA wants, what you must do, how you can deliver to their expectations and what relief you can expect

  • Training
  • 60 Minutes
  • Global
Develop, Execute and Enforce an Effective Validation Master Plan - Product Thumbnail Image

Develop, Execute and Enforce an Effective Validation Master Plan

  • Training
  • 60 Minutes
  • Global
How to prepare for the unannounced FDA compliance inspection - Product Thumbnail Image

How to prepare for the unannounced FDA compliance inspection

  • Training
  • 60 Minutes
  • Global
Monoclonal Antibodies and Therapeutic Proteins: Designing GLP Compliant Nonclinical Programs to Meet FDA Expectations - Product Thumbnail Image

Monoclonal Antibodies and Therapeutic Proteins: Designing GLP Compliant Nonclinical Programs to Meet FDA Expectations

  • Training
  • 60 Minutes
  • Global
Lean Documents and Document Control - Product Thumbnail Image

Lean Documents and Document Control

  • Training
  • 90 Minutes
  • Global
Hazard Analysis & Risk Management - New 14971 - Product Thumbnail Image

Hazard Analysis & Risk Management - New 14971

  • Training
  • 90 Minutes
  • Global
Why investigators often lose money in conducting sponsored clinical trials - Product Thumbnail Image

Why investigators often lose money in conducting sponsored clinical trials

  • Training
  • 60 Minutes
  • Global
4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan - Product Thumbnail Image

4-Region internal audits: Medical Device Quality System audits that cover internal regulatory compliance for FDA, Europe, Canada and Japan

  • Training
  • 60 Minutes
  • Canada, Japan, Europe Canada, Japan, Europe
GCP Audit of Clinical Evaluations for Japan: Requirements and expectations from the revised Japanese PAL - Product Thumbnail Image

GCP Audit of Clinical Evaluations for Japan: Requirements and expectations from the revised Japanese PAL

  • Training
  • 60 Minutes
  • Japan
Safety Risk Management for the Pharmaceutical Industry - Product Thumbnail Image

Safety Risk Management for the Pharmaceutical Industry

  • Training
  • 60 Minutes
  • Global
Preparing Compliant eCTD Submissions - Product Thumbnail Image

Preparing Compliant eCTD Submissions

  • Training
  • 60 Minutes
  • Global
'Performing effective supplier audits: a coming FDA compliance focus' - Product Thumbnail Image

'Performing effective supplier audits: a coming FDA compliance focus'

  • Training
  • Global
Practical tips to comply and implement the Adverse Event Reporting requirement of the new Dietary Supplement and Nonprescription Drug Consumer Protection Act - Product Thumbnail Image

Practical tips to comply and implement the Adverse Event Reporting requirement of the new Dietary Supplement and Nonprescription Drug Consumer Protection Act

  • Training
  • 60 Minutes
  • Global
Cleaning Validation - Chemical & Microbiological Aspects - Product Thumbnail Image

Cleaning Validation - Chemical & Microbiological Aspects

  • Training
  • 60 Minutes
  • Global
Key differences in Design Control Requirements between ISO13485:2003 and the FDA Quality System Regulation - Product Thumbnail Image

Key differences in Design Control Requirements between ISO13485:2003 and the FDA Quality System Regulation

  • Training
  • 60 Minutes
  • Global
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