Ganesh Nair
Ganesh Nair completed his graduation in law from IP university. He is an ardent researcher who has written various research papers and articles on contemporary legal issues. His keen interest in the field of research made him pursue a career in legal research. His core area of interest include Cyber, IPR and Finance laws.
What are FORMs COS-1 and COS-2
The Directorate General of Health Services authorises the Central Drugs Standard Control Organisation to issue cosmetic goods and product licenses. The drugs and cosmetics act 1940 and cosmetics rules 2020 are the two regulations that deal with cosmetic regulations in India. The government has emphasised these rules to ensure that safe, high grade and effective […]
BIS ISI certification for Feeding Bottle
What is BIS certification? Bureau of Indian standards issues the BIS certification. The BIS certification gives the customer guarantee of the product’s safety, quality and reliability. The BIS certification is mandatory for some products, especially the ones that affect public life and health. Till now, there are 380 products that need mandatory registration. The BIS […]
Licensing Authorities for Medical Device Product Registration in India
The medical device industry in India is growing rapidly, and it is expected that it shall continue to do so in the coming few years. As the Indian consumer is becoming more and more conscious about his health, there has been a huge demand for medical device production both domestically and internationally. The government had […]
What is a Free Sale Certificate?
A free sale certificate is a document issued for the export of medical equipment/devices, cosmetics and food items. These materials are not governed under the Drugs and Cosmetics act. The certificate states that the items mentioned in the certificate are safe. Further, they show these devices are sold without restrictions in the country of origin […]
BIS Certification for Wires& Cables
The BIS (Bureau of Indian standards) is responsible for assuring that the products in India attain the statutory standards before entering the market. The BIS has laid down various norms for the manufacturers of wires & cables. Recently the latest IS 17505 (part 1) was published in the gazette in the year 2021. This standard was introduced […]
BIS ISI Certification for kitchen appliances
Kitchen appliances are used in our day-to-day life. It is essential that these products are of good quality. The government has set ISI standards on these appliances to ensure that only safe products is utilised by the people. In this blog, we shall look into the process of obtaining BIS ISI certification for Kitchen appliances. […]
Registration of Software as Medical Device in India
With a view to expanding the scope of the regulations related to ‘medical devices,’ the government released a notification in the year 2020. This comes after the government introduced the Medical device rules in 2017. Before this, India had no specific regulation for medical devices; certain devices were just being regulated under the old Drugs […]
Difference between Notified & Non-Notified Medical Devices
CDSCO stands for Central Drugs Standard Control organisation. This entity is responsible for the regulation of drugs in India. CDSCO works under the ambit of the Directorate General of health services, which is governed by the Ministry of health and family welfare. CDSCO is responsible for conducting drug trials, keeping track of the quality of […]
BIS ISI certification for Automotive Tubes & Tyres
In the year 2011, the government made it mandatory for all the tyre manufacturers in India to meet the BIS standards for tyres. The dealers can only sell the tyres that carry the BIS mark on the sidewall. This mark is similar to the CE mark prevalent in the European Union. This BIS registration is […]
CDSCO Approval for Voluntary Registration of Medical Devices
In India, the regulation of medical devices is carried out by the Central Drugs Standard Control Organisation (CDSCO). The government authority has enlisted around 37 medical devices as per the latest notification. The CDSCO has made an amendment to the Medical device rules of 2017. The amendment stated that stakeholders could make a voluntary registration […]
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