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Dutch.pdf

laboratory-patient-journey-centrally-authorised-medicine_nl.pdf
Preview of Dutch
🔗 Source: ema.europa.eu
📊 Size: 1.76 MB
👤 Author: European Medicines Agency
⬇️ Downloads: 127

Summary

The European Medicines Agency (EMA) oversees the journey of a medicine from laboratory to patient, involving research, development, evaluation, authorisation, and safety monitoring. Pharmaceutical and biotechnology companies, doctors, and academics conduct initial research on tens of thousands of substances, with only a small number progressing to clinical trials. EMA provides scientific advice to support the development of high-quality medicines, ensuring that studies are scientifically sound and conducted ethically. The agency cannot influence which medicines are developed but publicises areas of need, such as new antibiotics, and provides incentives for researching rare diseases and medicines for children. Scientific advice helps developers design better studies, generating robust data to demonstrate a medicine's effectiveness and safety, ultimately benefiting patients.

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Description

The European Medicines Agency (EMA) oversees the journey of a medicine from laboratory to patient, involving research, development, evaluation, authorisation,...

Technical Information

  • File Format: PDF
  • File Size: 1.76 MB
  • Pages: 26
  • Language: EN
  • Author: European Medicines Agency
  • Total Downloads: 127
  • Last Updated: 1 day ago

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This PDF document about Dutch provides comprehensive information and guidance. Whether you're a beginner or advanced user, this resource offers valuable insights into Dutch.

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