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Pharmacovigilance Summer Internship

NTHRYS >> Services >> Academic Services >> Internships >> Summer Internships >> Pharmacovigilance Summer Internship

Pharmacovigilance Summer Internships

Join Pharmacovigilance summer internships to explore the monitoring and evaluation of drug safety, focusing on adverse drug reaction (ADR) reporting, drug safety surveillance, risk management, and the use of real-world data to improve patient outcomes.
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Proj / Publications
Back to All Summer Internships.
Join our Pharmacovigilance Publication Projects and earn co-authorship in the articles that will be published in Scopus Indexed or Science Citation Index (SCI) journals.

Focused Areas under Pharmacovigilance Summer Internship

  1. Adverse drug reaction (ADR) monitoring and reporting
  2. Drug safety surveillance and risk management
  3. Pharmacovigilance in clinical trials
  4. Post-marketing surveillance of drug safety
  5. Real-world data analysis for drug safety monitoring
  6. Pharmacovigilance in personalized medicine
  7. Risk-benefit analysis of drugs
  8. Regulatory frameworks for pharmacovigilance
  9. Pharmacovigilance of biologics and biosimilars
  10. Signal detection and risk assessment in pharmacovigilance
  11. Pharmacovigilance in pediatric and geriatric populations
  12. Drug safety monitoring in rare diseases
  13. Pharmacovigilance in cancer therapies
  14. Pharmacovigilance in vaccines and immunotherapies
  15. Applications of artificial intelligence in pharmacovigilance
  16. Pharmacogenetics in pharmacovigilance
  17. Pharmacovigilance in cardiovascular drugs
  18. Data mining and statistical analysis in drug safety
  19. Case report management in pharmacovigilance
  20. International standards and guidelines in pharmacovigilance

Protocols Covered across various focussed areas under Pharmacovigilance Summer Internship

  1. Adverse drug reaction reporting protocols
  2. Pharmacovigilance risk management workflows
  3. Post-marketing surveillance data collection techniques
  4. Signal detection methods in pharmacovigilance
  5. Real-world data integration for drug safety analysis
  6. Pharmacovigilance reporting protocols for biologics
  7. Risk-benefit analysis techniques in drug safety monitoring
  8. Pharmacovigilance case report processing workflows
  9. Regulatory compliance protocols in pharmacovigilance
  10. Pharmacovigilance data mining and statistical analysis techniques

Duration: 5, 10, 15, 20, and 30 Days

Note: Please cross confirm whether internship slots for this field are available before joining.

Click Here for Pharmacovigilance Summer Internship
Application Process and Other info


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