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Results for tag: "Regulatory Affairs"

FDA Vs Health Canada - Product Thumbnail Image

FDA Vs Health Canada

  • Training
  • 60 Minutes
  • Canada
Computer System Validation and Part 11 Compliance - Product Thumbnail Image

Computer System Validation and Part 11 Compliance

  • Training
  • 60 Minutes
  • Global
21 CFR 11 Compliance for Excel Spreadsheet - Product Thumbnail Image

21 CFR 11 Compliance for Excel Spreadsheet

  • Training
  • 90 Minutes
  • Global
Effective Training Practices for FDA Compliance - Product Thumbnail Image

Effective Training Practices for FDA Compliance

  • Training
  • 75 Minutes
  • Global
Conducting Effective Mock FDA Inspections - Product Thumbnail Image

Conducting Effective Mock FDA Inspections

  • Training
  • 90 Minutes
  • Global
FDA Inspections: What Regulations Expect - Product Thumbnail Image

FDA Inspections: What Regulations Expect

  • Training
  • 90 Minutes
  • Global
Preparing for a U.S. FDA Audit - Product Thumbnail Image

Preparing for a U.S. FDA Audit

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

Preparing Compliant eCTD Submissions

  • Training
  • 60 Minutes
  • Global
Pharmaceutical Manufacturing Process Validation - Product Thumbnail Image

Pharmaceutical Manufacturing Process Validation

  • Training
  • 60 Minutes
  • Global
Change Control - Implementation and Management - Product Thumbnail Image

Change Control - Implementation and Management

  • Training
  • 60 Minutes
  • Global
Master Planning for Computer System Validation - Product Thumbnail Image

Master Planning for Computer System Validation

  • Training
  • 60 Minutes
  • Global
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Regulatory Affairs in the biotechnology industry is the process of obtaining and maintaining approval from regulatory authorities for the development, manufacture, and marketing of biotechnology products. This includes the submission of applications, such as Investigational New Drug (IND) applications, New Drug Applications (NDAs), and Biologics License Applications (BLAs). Regulatory Affairs professionals are responsible for ensuring that biotechnology products comply with applicable laws and regulations. Regulatory Affairs professionals must have a thorough understanding of the regulatory environment and the ability to interpret and apply regulations to the development and marketing of biotechnology products. They must also be able to effectively communicate with regulatory authorities and other stakeholders. Companies in the Regulatory Affairs market in the biotechnology industry include Parexel, Quintiles, Covance, PRA Health Sciences, and Charles River Laboratories. Show Less Read more