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Results for tag: "Regulatory Affairs"

The FDA Inspection Process: From SOP to 483 - Product Thumbnail Image

The FDA Inspection Process: From SOP to 483

  • Training
  • 60 Minutes
  • Global
Analytical Method Validation and Transfer - Product Thumbnail Image

Analytical Method Validation and Transfer

  • Training
  • 90 Minutes
  • Global
Risk Based Monitoring for GCP Compliance - Product Thumbnail Image

Risk Based Monitoring for GCP Compliance

  • Training
  • 60 Minutes
  • Global
CDISC Mapping 2: ODM, MindMaps and References - Product Thumbnail Image

CDISC Mapping 2: ODM, MindMaps and References

  • Training
  • 90 Minutes
  • Global
ICH Stability Requirements and Challenges - Product Thumbnail Image

ICH Stability Requirements and Challenges

  • Training
  • 60 Minutes
  • Global
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Writing Excellent SOPs - Webinar (Recorded) - Product Thumbnail Image

Writing Excellent SOPs - Webinar (Recorded)

  • Webinar
  • May 2023
  • 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