Summary
Overview
Work History
Education
Skills
PROJECT
Certification
HOBBIES and INTRESTS
LANGUAGE
Timeline
Generic
Anupriya Asati

Anupriya Asati

Ghaziabad

Summary

Dedicated M. Pharm graduate specialized in Pharmacology, blending robust experience in Medical Device Vigilance, Clinical Research, and Medical Summarization. Eagerly seeking a challenging career opportunity to leverage Materiovigilance expertise, clinical acumen, and comprehensive training for the advancement of the company's objectives. Known for diligent work ethic, self-motivation, and an insatiable appetite for learning. A collaborative team player with a proactive and positive mindset, poised to deliver tangible contributions to organizational success.

Overview

3
3
years of professional experience
1
1
Certification

Work History

Jr. MATERIOVIGILANCE ASSOCIATE

INDIAN PHARMACOPOEIA COMMISION
Ghaziabad
06.2023 - Current
  • Analyzing and processing ICSR in the database to the national materiovigilance center.
  • Actively monitoring adverse events related to medical devices. Collection and analysis of adverse event reports associated with medical devices received from MAHs, and Medical Device License Holders.
  • Knowledge on regulation of medical devices in India (Medical device Rules, 2017) and international regulations (USFDA, TGA, Health Canada).
  • Facilitating communication and collaboration between various stakeholders involved in materiovigilance, including healthcare professionals, regulatory authorities, manufacturers, and consumers.
  • Updated and managed the MVPI E-newsletter, providing stakeholders, healthcare professionals, and regulatory professionals with timely information on materiovigilance updates, trends, and regulatory changes.
  • Organized and coordinated seminars, conferences, and meetings related to materiovigilance and medical device safety, including planning, logistics, and content development, to ensure successful and informative events.
  • To provide guidance and support to the project trainees under MvPI for the completion of their projects on the safety of medical devices.

CLINICAL RESEARCH ASSOCIATE

PATANJALI RESEARCH INSTITUTE
Haridwar
09.2022 - 06.2023
  • Developing and writing trial protocols, as well as locating and assessing feasible sites.
  • Liaison with the doctor and investigator for conducting the trial.
  • Designing, collecting, and verifying data entered in the CRF.
  • Archive study documentation, prepare final reports, and occasionally manuscripts for publication.

Senior Medical Summarizer

Innodata India Pvt. Ltd.
12.2021 - 09.2022
  • Scrutinize medical records and related documents and proactive in identifying and resolving errors
  • Documented patient's medical histories, complaints and treatment rendered
  • Strong knowledge of medical terminology/diseases, their symptoms and treatment/ impact of medicines etc
  • Substantiate the symptoms, treatment and prognosis of illness based on records available.

Education

M. Pharm Phramacology -

Guru Ghasidas Vishwavidyalaya, Bilaspur (C.G)
08.2021

B.Pharm -

Shri Ram Institute of Technology, Jabalpur (M.P)
07.2018

Skills

  • Experience with ICSR
  • Adverse event reporting
  • Regulatory compliance
  • Risk assessment
  • Literature review
  • Data collection and analysis
  • Identifying trends and patterns
  • Database management for adverse event reporting
  • Compliance with regulatory requirements
  • Stakeholder engagement
  • Oral communication
  • Preparing reports
  • Protocol development
  • Site assessment
  • Knowledge of clinical trial phases, preclinical research, and drug discovery processes
  • PowerPoint: Presentation creation
  • Word: Documentation and report writing
  • Collaborative and effective team player
  • Eagerness to learn new skills and technologies
  • Reliable and detail-oriented in all tasks

PROJECT

  • M. Pharm

Preclinical estimation of Isoliquiritigenin in impeding the succession of succession of inflammation and angiogenesis on uveitic glaucoma.

  • B. Pharm

UV Estimation of Carvedilol

Certification

  • PMDA-ATC Pharmacovigilance Webinar 2024
  • Training on PMDA-ATC E-learning Training Course: Medical Devices Review.
  • Completed four months of online training from CLINI-INIDA Clinical research, Clinical Data Management, Pharmacovigilance, Medical Writing, Drug Regulatory Affairs.
  • Base SAS certification cource from SAS Institute Online
  • Awards received: Earned young scientist award on international conference on latest trends and innovations in pharmaceutical and biosciences.
  • Successfully completed 1 month training work at Day Mark Pharmaceuticals in manufacturing Basic Formulation.
  • Attended several national and international seminars and webinars related to Pharmacology, drug discovery and drug delivery.

HOBBIES and INTRESTS

  • Professional Networking
  • Event Planning
  • Meditation or Mindfulness
  • Gardening

LANGUAGE

  • Hindi
  • English

Timeline

Jr. MATERIOVIGILANCE ASSOCIATE

INDIAN PHARMACOPOEIA COMMISION
06.2023 - Current

CLINICAL RESEARCH ASSOCIATE

PATANJALI RESEARCH INSTITUTE
09.2022 - 06.2023

Senior Medical Summarizer

Innodata India Pvt. Ltd.
12.2021 - 09.2022

M. Pharm Phramacology -

Guru Ghasidas Vishwavidyalaya, Bilaspur (C.G)

B.Pharm -

Shri Ram Institute of Technology, Jabalpur (M.P)

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Anupriya Asati