[PDF][PDF] Role of pharmacovigilance in India: An overview
SG Suke, P Kosta, H Negi - Online journal of public health informatics, 2015 - ojphi.jmir.org
Pharmacovigilance (PV) plays a key role in the healthcare system through assessment,
monitoring and discovery of interactions amongst drugs and their effects in human …
monitoring and discovery of interactions amongst drugs and their effects in human …
Development of pharmacovigilance system in India and paradigm of pharmacovigilance research: an overview
P Singh, Y Vaishnav, S Verma - Current Drug Safety, 2023 - ingentaconnect.com
The drugs are projected to cure, prevent and treat diseases; however, there are also
chances of mild or severe adverse drug reactions (ADRs) in the patients. Pharmacovigilance …
chances of mild or severe adverse drug reactions (ADRs) in the patients. Pharmacovigilance …
[PDF][PDF] Pharmacovigilance process in India: An overview
PN Amale, SA Deshpande, YD Nakhate, NA Arsod - J Pharmacovigil, 2018 - academia.edu
Clinical trial study of drug generally detects common Adverse Drug Reaction (ADR) but, the
reaction which occurs after long duration in a specific person or population remains …
reaction which occurs after long duration in a specific person or population remains …
Pharmacovigilance in India in comparison with the USA and European Union: Challenges and perspectives
J Jose, NR Rafeek - Therapeutic innovation & regulatory …, 2019 - journals.sagepub.com
Pharmacovigilance (PV) is an integral part of the drug regulation system. PV plays an
indispensable role in the identification, assessment, and publicizing of adverse drug …
indispensable role in the identification, assessment, and publicizing of adverse drug …
Strategy support for the Post‐Market Monitoring (PMM) of GM plants: Review of existing PMM strategies developed for the safety assessment of human and animal …
ADAS UK ltd - EFSA Supporting Publications, 2015 - Wiley Online Library
ABSTRACT Commission Implementing Regulation (EU) No 503/2013 on applications for
authorisation of genetically modified (GM) food and feed legalised the requirement for a Post …
authorisation of genetically modified (GM) food and feed legalised the requirement for a Post …
Pharmacovigilance-A Master Key for Drug Safety
M Jaani, ND Venkatesh - Journal of Pharmaceutical Sciences …, 2019 - search.proquest.com
biggest member in the world with 500 API's [5] 2.[24] Starting of a pharmacovigilance center:
A pharmacovigilance system has now started emerging in order to address the adverse …
A pharmacovigilance system has now started emerging in order to address the adverse …
[图书][B] COVID-19: An Opportunity to Revamp Pharmacovigilance System
Traditional medicine (TM) is considered one of the major verticals of the healthcare system
across the globe for more comfortable affordability and accessibility than conventional …
across the globe for more comfortable affordability and accessibility than conventional …
The case for a niche pharmacovigilance system relating to drug provision and distribution in resource limited settings: Presented by the development of a requirement …
B Huysamen, IH de Kock, L Bam - 2019 IEEE International …, 2019 - ieeexplore.ieee.org
In the contemporary healthcare landscape, the implementation of innovative drug
manufacturing and distribution systems is becoming increasingly prominent in developing …
manufacturing and distribution systems is becoming increasingly prominent in developing …
[PDF][PDF] Journal of Pharmacovigilance and Drug Research
M Manna, A Shil - Journal of Pharmacovigilance and Drug Research, 2020 - academia.edu
Results: In many cases, the increase in therapeutic doses and treatment duration is
accompanied by the occurrence of severe side effects. Taking into account the huge …
accompanied by the occurrence of severe side effects. Taking into account the huge …
[HTML][HTML] Pharmacovigilance in generic Indian pharmaceutical industries-Need of the moment
P Rajpurohit, M Suva, H Rajpurohit… - … of Pharmacovigilance and …, 2021 - jpadr.com
Introduction: The pharmacovigilance department is liable for monitoring the safety of
medicines during clinical trials and normal clinical use. The necessity of the …
medicines during clinical trials and normal clinical use. The necessity of the …