Wednesday, December 2, 2020

Medical Device Manufacturing | consultant – Operon strategist



Medical Device Manufacturing

A medical device is a gadget, material, software or an apparatus which can be used alone or in combinations, including the product proposed by the medical device manufacturer to be utilized particularly for diagnostic or potentially for therapeutic purposes. And required for its proper application, planned by the Medical Device manufacturers to be utilized for people. Medical devices differ as per their planned use and indication. For example, medical devices like tongue depressors, medical thermometers and disposable gloves to its advanced devices such as computers which help with the control of medical testing, implants, and prostheses. The design plan of medical device constitutes an important section of the field of biomedical designing.

Medical Device Manufacturing in India

There is the national regulatory body like CDSCO for Indian medical devices and pharmaceuticals, it is the licensing authority. The role of CDSCO is to provide the approval to any new medical device which is in the process to be imported to India. Within CDSCO, Drug Controller General of India (DCGI) is the final authority and controls medical devices and pharmaceuticals. Drug Controller General of India is in charge of endorsement of licenses of particular categories of Drugs such as IV-Fluids, blood and blood products, Vaccines and all medical devices. The Medical device manufacturing process is classified and categorized under the CDSCO guideline.

Medical Devices Manufacturing in the US

Under the Food, Drug, and Cosmetic Act, the U.S. Food and Drug Administration recognizes three classes of medical devices, based on the level of control necessary to assure safety and effectiveness. The classification procedures are described in the Code of Federal Regulations, Title 21, part 860 (usually known as 21 CFR 860). The USFDA allows Medica device marketing in two different processes. Most common to be 510(k) process and second is Premarket Approval process, in the case of Premarket approval, clinical trials are required  

Read More Article - 

1.Orthopedic Implants Manufacturing

2.Dental Implants Manufacturing

3.Blood Collection Tubes Manufacturing

4. How to start the Manufacturing of Disposable Syringes?

5. disposable syringe manufacturers

Contact details –

Phone  no -  93702 83428

Mail id – enquiry@operonstrategist.com

If  You Want Medical Devices Services Consultation For Following.


No comments:

Post a Comment

CDSCO Import License for Medical Devices In India

  Central Drugs Standard Control Organisation is, known as CDSCO, is a regulatory body for the Indian medical devices industry, under the vi...