OVERVIEW OF PHARMACOVIGILANCE AND THEIR ICH GUIDELINES

  • Unique Paper ID: 169820
  • Volume: 11
  • Issue: 6
  • PageNo: 2410-2412
  • Abstract:
  • Pharmacovigilance, the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug- related problems, is intrinsically linked to effective information management. The evolution of data sources, emphasizing the integration of electronic health records, wearable devices and real world evidence to enhance the depth and breadth of information available for analysis. How those tools are utilized to sift through vast datasets, identifying potential safety concerns and aiding regulatory decision-making. Furthermore, the abstract delves into the importance of structured information sharing between regulatory agencies, pharmaceutical companies, healthcare providers. Pharmacovigilance play an important role in the healthcare system through monitoring and interaction of drugs and there effects in the human body. In this article includes good manufacturing practices (GCP) and (ICH) guidelines for pharmaceuticals for human use are examined as an important aspects in the transformation of clinical trial to the objective of pharmacovigilance in pharmaceutical production India becomes third largest country in the world.

Cite This Article

  • ISSN: 2349-6002
  • Volume: 11
  • Issue: 6
  • PageNo: 2410-2412

OVERVIEW OF PHARMACOVIGILANCE AND THEIR ICH GUIDELINES

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