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Results for tag: "Regulatory Affairs"

Fill-Finish Manufacturing Market Report 2025-2035 - Product Thumbnail Image

Fill-Finish Manufacturing Market Report 2025-2035

  • Report
  • July 2025
  • 236 Pages
  • Global
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ADC Drug CDMO Service Market - Global Forecast 2026-2032 - Product Thumbnail Image

ADC Drug CDMO Service Market - Global Forecast 2026-2032

  • Report
  • January 2026
  • 190 Pages
  • Global
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Chemical Drug CDMO Market - Global Forecast 2026-2032 - Product Thumbnail Image

Chemical Drug CDMO Market - Global Forecast 2026-2032

  • Report
  • January 2026
  • 196 Pages
  • Global
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3D Printed Drugs Market - Global Forecast 2026-2032 - Product Thumbnail Image

3D Printed Drugs Market - Global Forecast 2026-2032

  • Report
  • January 2026
  • 187 Pages
  • Global
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Unit Dose Manufacturing Market - Global Forecast 2026-2032 - Product Thumbnail Image

Unit Dose Manufacturing Market - Global Forecast 2026-2032

  • Report
  • January 2026
  • 183 Pages
  • 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