Copyright © 2026 Authors retain the copyright of this article. This article is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

@article{187257,
        author = {Pratiksha Sanjay Chende and Suhas Rajendra Khandagale and Supriya khivaraj Bhagat and Dr. Nilesh O. Chachda},
        title = {PHARMACOVIGILANCE: DIGITAL ERA},
        journal = {International Journal of Innovative Research in Technology},
        year = {2025},
        volume = {12},
        number = {6},
        pages = {5062-5076},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=187257},
        abstract = {Pharmacovigilance is an important and crucial part of clinical research. Pharmacovigilance is the branch of pharmaceutical research that deals with the detection, assessment, understanding, and avoidance of drug adverse effects, particularly those that are short- and long-term. It is the investigation of the safety of commercially available medications in real world clinical usage scenarios in sizable populations. Pharmacovigilance is an important and vital part of clinical research. Throughout a product's lifecycle, post- marketing pharmacovigilance and clinical trial safety are crucial.},
        keywords = {Adverse drug reaction, Clinical trials phases, MedDRA dictionary, Patient safety, SUSAR,  SUGAM.},
        month = {November},
        }