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Results for tag: "Regulatory Affairs"

Quality Planning Process and Procedure - Product Thumbnail Image

Quality Planning Process and Procedure

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

Pharmaceutical Manufacturing Process Validation

  • Training
  • 60 Minutes
  • Global
Best Practices in 510(k) Submissions - Product Thumbnail Image

Best Practices in 510(k) Submissions

  • Training
  • 60 Minutes
  • Global
An Overview of Design and Development Planning - Product Thumbnail Image

An Overview of Design and Development Planning

  • Training
  • 60 Minutes
  • Global
Parallel Scientific Advice: How effective is the system established between the EMEA and the FDA - Product Thumbnail Image

Parallel Scientific Advice: How effective is the system established between the EMEA and the FDA

  • Training
  • 60 Minutes
  • Middle East, Africa, Europe Middle East, Africa, Europe
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
Best Documentation Practices for FDA Compliance - Product Thumbnail Image

Best Documentation Practices for FDA Compliance

  • Training
  • 60 Minutes
  • Global
Good Laboratory Practices for Food Manufacturing - Product Thumbnail Image

Good Laboratory Practices for Food Manufacturing

  • Training
  • 90 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