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Current Status of the Regulation for Medical Devices

In the light of escalating use of medical devices, stringent regulatory standards are required to ensure that the devices are safe, well studied and have least adverse reactions. Recently introduced guidelines and the amendment in the law will provide adequate guidance for both the manufacturers and...

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Detalles Bibliográficos
Autores principales: Shah, Anuja R., Goyal, R. K.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040860/
https://www.ncbi.nlm.nih.gov/pubmed/21369427
http://dx.doi.org/10.4103/0250-474X.49085
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author Shah, Anuja R.
Goyal, R. K.
author_facet Shah, Anuja R.
Goyal, R. K.
author_sort Shah, Anuja R.
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description In the light of escalating use of medical devices, stringent regulatory standards are required to ensure that the devices are safe, well studied and have least adverse reactions. Recently introduced guidelines and the amendment in the law will provide adequate guidance for both the manufacturers and competent authorities to manage cases efficiently and appropriately. India has emerged as one of the leaders in pharmaceutical industry. Like many other amendments in Drugs and Cosmetics Act that have boosted the global confidence in pharmaceutical industry in India, guidelines for devices will encourage the much needed research in medical devices. Pharmacy personnel can certainly play an important role in the regulation of medical devices. Safety, risks, effectiveness and performance of the medial devices need to be well established and regulated properly. It is hoped that the guidelines are implemented and regulated properly with effective outcome.
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spelling pubmed-30408602011-03-02 Current Status of the Regulation for Medical Devices Shah, Anuja R. Goyal, R. K. Indian J Pharm Sci Review Article In the light of escalating use of medical devices, stringent regulatory standards are required to ensure that the devices are safe, well studied and have least adverse reactions. Recently introduced guidelines and the amendment in the law will provide adequate guidance for both the manufacturers and competent authorities to manage cases efficiently and appropriately. India has emerged as one of the leaders in pharmaceutical industry. Like many other amendments in Drugs and Cosmetics Act that have boosted the global confidence in pharmaceutical industry in India, guidelines for devices will encourage the much needed research in medical devices. Pharmacy personnel can certainly play an important role in the regulation of medical devices. Safety, risks, effectiveness and performance of the medial devices need to be well established and regulated properly. It is hoped that the guidelines are implemented and regulated properly with effective outcome. Medknow Publications 2008 /pmc/articles/PMC3040860/ /pubmed/21369427 http://dx.doi.org/10.4103/0250-474X.49085 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Shah, Anuja R.
Goyal, R. K.
Current Status of the Regulation for Medical Devices
title Current Status of the Regulation for Medical Devices
title_full Current Status of the Regulation for Medical Devices
title_fullStr Current Status of the Regulation for Medical Devices
title_full_unstemmed Current Status of the Regulation for Medical Devices
title_short Current Status of the Regulation for Medical Devices
title_sort current status of the regulation for medical devices
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040860/
https://www.ncbi.nlm.nih.gov/pubmed/21369427
http://dx.doi.org/10.4103/0250-474X.49085
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