Regulatory guidelines for medical devices in India: An overview

Main Article Content

Nadimpalli Radhadevi
Veeranna Balamuralidhara
Teggina Math Pramod Kumar
Valluru Ravi

Abstract

The objective of the present study offers an overview of regulatory guidelines for medical devices in India. Medical devices are now a pervasive part of modern medical care. They are in many cases associated with quality of care. In some cases, the use of devices has certainly improved quality. In other cases, devices have been associated with many problems. The approach to quality of devices has depended largely on regulation. 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. While these regulations and reforms promise to clarify, unify, and expedite the process of manufacturing and importing medical devices into India, they also pose their own challenges and complications. Understanding the regulatory
reforms imminent in India will be crucial for foreign companies looking to enter or expand their business in India’s medical markets. It is hoped that the guidelines are implemented and regulated properly with effective outcome.This article highlights current regulations pertaining to applications for medical device registration certificates, medical device clinical trials, and
medical device manufacturing/importation licenses.

Downloads

Download data is not yet available.

Article Details

How to Cite
Radhadevi, N., Balamuralidhara, V., Kumar, T. M. P., & Ravi, V. (2014). Regulatory guidelines for medical devices in India: An overview. Asian Journal of Pharmaceutics (AJP), 6(1). https://doi.org/10.22377/ajp.v6i1.68
Section
Articles

References

Jeffery DB. The regulation of medical devices and the role of the medical

devices agency. Br J Clin Pharmacol 2001;52:229-35.

Ghorbel M, Samet M, Hamida A, Tomas A. Fully integrated and versatile

CMOS micro stimulator dedicated to Cochlear Implant. J Appl Sci

;6:2978-90.

Schedule-MIII. Requirements for the manufacture, import and sale of

medical devices. [Sited 2009 Feb 23]. Available from: http://cdsco.nic.

in/Medical_Devices_Guidelines.pdf.

Anuja R Shah, Goyal RK. Status of the regulation for medical devices.

Indian J Pharmal Sci 2008;70:695-700.

Hala A, Farrag. Post irradiation effect on adherent growth, Slime

formation and antibiotic resistance of pseudomonas aeruginosa causing

human infection. J Med Sci 2001;1:244-50.

Ananthan G, Sivaperumal P, Hussain MS. Antibacterial potential

of marine ascidian phallusia arabica against isolated urinary tract

infections bacterial pathogens. Asian J Anim Sci 2011;5:208-12.

Malmoe R, Alumax A, Baroque NK. Knowledge on the Move. J Appl Sci

;11:3062-9.

Matthew CO, Monica A. E-Readiness of Enugu state, Nigeria. Asian J

Inform Manag 2011;5:25-34.

Armani A, Gregorian. Case study of the size, causes and consequences

of shadow Economy (On the example of the Republic of Armenia).

Trends Appl Sci Res 2007;2:365-73.

Fazal-e-Amin, Mahmood AK, Oxley A. Oriented implementation of

software product lines components. Inform Technol J 2010;9:1262-9.

Guidelines for import and manufacture of medical devices [Internet].

India. CDSCO; Accessed on 2009 February. Available from: http://cdsco.

nic.in/medical%20device%20A42.html.

Shet R. Keeping in step with global medical device regulations.

[Internet]. 2009 [cited 2012 Apr 23]. Available from: http://www.

expresspharmaonline.com/20091231/ipcspecial08.shtml.

Gross A, Hirose M. Updates on the Medical Device Regulations in India.

Medical Product Outsourcing. [Internet]. 2009 [cited 2012 Apr 23].

Availableat from: http://www.pacificbridgemedical.com/publications/

india/2009_updates_on_medevice_regs_india.

Kabir A, Islam MS, Ahmed MS, Barbhuiya K. Factors influencing infant

and child mortality in Bangladesh. J Med Sci 2001;5:292-5.

Guidance document on common submission format for import license

in10 of medical devices in India [Internet]. India. CDSCO, 2010 August

th. Available from: http://cdsco.nic.in/Guidance.PDF.

Ames Gross and Arthur Chan. India’s latest medical device regulation.

developments. Pacific Bridge Medical. [Internet] [Cited on 23/4/2012].

Available from: http://www.medicaldevices.org/sites/default/files/

India%20Medical%20Device%20Regulations.pdf.

Requirements for conducting clinical trial(s) of medical devices in India.

[Internet]. India. CDSCO. 2010 August 4th. Available from: http://cdsco.

nic.in/Requirements%20for%20Conducting%20Clinical%20Trial(s)%20

of%20Medical%20Devices%20in%20India.PDF.

Guidance document on application for grant of Licence in Form-28 for manufacture of Medical Devices in India under CLAA Scheme. [Internet].India. CDSCO; 2010 August 12th. Available from: http://cdsco.nic.inGuidance%20document%20on%20application%20for%20grant%20of%20Licence%20in%20Form28%20for%20manufacture%20of%20Medical%20Devices%20in%20India%20under%20CLAA%20Scheme.PDF.