+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)

Results for tag: "Pharmaceutical Regulation"

Creating Effective SOPs for Regulatory Compliance - Product Thumbnail Image

Creating Effective SOPs for Regulatory Compliance

  • Training
  • 60 Minutes
  • Global
Qualification and Audit of Suppliers and Vendors - A Risk Based Approach - Product Thumbnail Image

Qualification and Audit of Suppliers and Vendors - A Risk Based Approach

  • Training
  • 90 Minutes
  • Global
Pharmaceutical Regulations Training Bundle for Regulatory Affairs Professionals - Product Thumbnail Image

Pharmaceutical Regulations Training Bundle for Regulatory Affairs Professionals

  • Training
  • 7 Hours
  • Global
FDA: Mock and Pre-Approval Inspections (PAIs) - Part II - Product Thumbnail Image

FDA: Mock and Pre-Approval Inspections (PAIs) - Part II

  • Training
  • 120 Minutes
  • Global
Drug Manufacturing Inspection Part III - Product Thumbnail Image

Drug Manufacturing Inspection Part III

  • Training
  • 120 Minutes
  • Global
FDA Inspections: Understanding the Core Elements - Part I - Product Thumbnail Image

FDA Inspections: Understanding the Core Elements - Part I

  • Training
  • 120 Minutes
  • Global
Best Practices for an Effective Cleaning Validation Program - Product Thumbnail Image

Best Practices for an Effective Cleaning Validation Program

  • Training
  • 60 Minutes
  • Global
Annex 1 Chapter 6 and its Comparison to Compendial Mandates: What Does It Imply to the Industry - Product Thumbnail Image

Annex 1 Chapter 6 and its Comparison to Compendial Mandates: What Does It Imply to the Industry

  • Training
  • 60 Minutes
  • Global
Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology - Product Thumbnail Image

Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology

  • Training
  • 120 Minutes
  • Global
Design History Files and Technical Files under US FDA and EU MDD - Product Thumbnail Image

Design History Files and Technical Files under US FDA and EU MDD

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Equipment Qualification and Process Validation - Product Thumbnail Image

Equipment Qualification and Process Validation

  • Training
  • 90 Minutes
  • Global
Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3 - Product Thumbnail Image

Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3

  • Training
  • 90 Minutes
  • Global
Drug Labeling and Packaging: Meeting Regulatory Requirements - Product Thumbnail Image

Drug Labeling and Packaging: Meeting Regulatory Requirements

  • Training
  • 60 Minutes
  • Global
Risk Management of Raw Materials in a GMP Environment - Product Thumbnail Image

Risk Management of Raw Materials in a GMP Environment

  • Training
  • 90 Minutes
  • Global
How to Write Error Free and FDA Compliant Procedures - Product Thumbnail Image

How to Write Error Free and FDA Compliant Procedures

  • Training
  • 90 Minutes
  • Global
European Filing and Registration Procedures - Product Thumbnail Image

European Filing and Registration Procedures

  • Training
  • 90 Minutes
  • Europe
Process Validation - Current Industry Practices and FDA Guidance Document Review - Product Thumbnail Image

Process Validation - Current Industry Practices and FDA Guidance Document Review

  • Training
  • 60 Minutes
  • Global
Understanding Disinfection and Cleanroom cleaning in a FDA Regulated Environment - Product Thumbnail Image

Understanding Disinfection and Cleanroom cleaning in a FDA Regulated Environment

  • Training
  • 90 Minutes
  • Global
Russia: Compliance Processes and Regulations - Product Thumbnail Image

Russia: Compliance Processes and Regulations

  • Training
  • 90 Minutes
  • Russia
Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan - Product Thumbnail Image

Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan

  • Training
  • 60 Minutes
  • Global
Loading Indicator

The Pharmaceutical Regulation market is a sector of the pharmaceutical industry that focuses on the regulation of drugs and other related products. It is responsible for ensuring that drugs are safe and effective for use by the public. This includes the evaluation of clinical trials, the approval of new drugs, and the monitoring of drug safety and efficacy. The market also includes the enforcement of regulations and the enforcement of intellectual property rights. The Pharmaceutical Regulation market is composed of a variety of stakeholders, including pharmaceutical companies, regulatory authorities, and research institutions. Pharmaceutical companies are responsible for the development and production of drugs, while regulatory authorities are responsible for the approval and monitoring of drugs. Research institutions are responsible for conducting clinical trials and providing data to regulatory authorities. Some of the major companies in the Pharmaceutical Regulation market include Pfizer, Merck, GlaxoSmithKline, Novartis, and Johnson & Johnson. Show Less Read more