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Drug Discovery Market Research Reports

Quality Expectations for Drugs and Biologics during Early Development: Phase 2 - Product Thumbnail Image

Quality Expectations for Drugs and Biologics during Early Development: Phase 2

  • Training
  • 75 Minutes
  • Global
Using Electronic Health Records and Claims Databases for Rapid-Response Pharmacovigilance Studies - Product Thumbnail Image

Using Electronic Health Records and Claims Databases for Rapid-Response Pharmacovigilance Studies

  • Training
  • 60 Minutes
  • Global
Getting the Most Out Of Data Mining for Pharmacovigilance and Risk Management - Product Thumbnail Image

Getting the Most Out Of Data Mining for Pharmacovigilance and Risk Management

  • Training
  • 60 Minutes
  • Global
Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms - Product Thumbnail Image

Designing an Effective Cleaning and Disinfection Program for Pharmaceutical, Biotech, and Medical Device Cleanrooms

  • Training
  • 90 Minutes
  • Global
Investigator responsibility/Legal commitment in drug and device clinical research: the reality - Product Thumbnail Image

Investigator responsibility/Legal commitment in drug and device clinical research: the reality

  • Training
  • 90 Minutes
  • Global
Data and Safety Monitoring in Clinical Research Involving Human Subjects - When and How - Product Thumbnail Image

Data and Safety Monitoring in Clinical Research Involving Human Subjects - When and How

  • Training
  • 90 Minutes
  • Global
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
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
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
  • Europe, Japan, Canada Europe, Japan, Canada
'Performing effective supplier audits: a coming FDA compliance focus' - Product Thumbnail Image

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

  • Training
  • Global
Designing Regulatory - Compliant Clinical Research Data Management Systems - Product Thumbnail Image

Designing Regulatory - Compliant Clinical Research Data Management Systems

  • 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
Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements - Product Thumbnail Image

Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements

  • Training
  • 90 Minutes
  • Global
Creating a Quality Assurance Program for (Clinical) Research Sites - Product Thumbnail Image

Creating a Quality Assurance Program for (Clinical) Research Sites

  • Training
  • 60 Minutes
  • Global
Auditing the QC Microbiology Laboratory for FDA Compliance - Product Thumbnail Image

Auditing the QC Microbiology Laboratory for FDA Compliance

  • Training
  • 75 Minutes
  • Global
FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance - Product Thumbnail Image

FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance

  • Training
  • 60 Minutes
  • Global
Implementation and Utilization of Standard Operating Procedures (SOPs) at the Clinical Research Site - Product Thumbnail Image

Implementation and Utilization of Standard Operating Procedures (SOPs) at the Clinical Research Site

  • Training
  • 60 Minutes
  • Global
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The Drug Discovery market is a sector of the pharmaceutical industry that focuses on the research and development of new drugs. It involves the identification of potential drug targets, the synthesis of new compounds, and the testing of these compounds for efficacy and safety. Companies in this market use a variety of techniques, such as high-throughput screening, computer-aided drug design, and molecular modeling, to identify and develop new drugs. The Drug Discovery market is highly competitive, with many large pharmaceutical companies and biotechnology firms competing for market share. Some of the major players in this market include Pfizer, Merck, Novartis, GlaxoSmithKline, AstraZeneca, Sanofi, Johnson & Johnson, Bristol-Myers Squibb, and Eli Lilly. Show Less Read more