Snehita Shukla

The working and functioning of businesses in India are governed by the Companies Act 2013. The regulators have set up distinct rules for One Person Company and Public Company, based on various factors such as ownership rights, transferability rights, Membership rights and so on. The difference between both them can be understood in detail below. […]

The Ministry of Information and technology passed an order on 18th March 2021, titled “Electronics and Information Technology Goods (Requirements for Compulsory Registration) Order, 2021.” which informed that the goods specified in the schedule mentioned in the order must bear the ‘Standard mark’ under the  Bureau of Indian Standards under Scheme II of Schedule II […]

The Ministry of Information and technology notified about a new order titled “Electronics and Information Technology Goods (Requirements for Compulsory Registration) Order, 2021.” on 18th March 2021. It notified that the goods specified in the order schedule must carry the ‘Standard mark’ under Scheme II of Schedule II of the Bureau of Indian Standards – […]

The Ministry of Electronic and Information Technology issued a notification on 17th August 2017, notifying about the products which are to be included in the schedule of Electronic and Information Technology Goods (Requirements for Compulsory Registration) Order, 2012. There is an inclusion of 13 goods to the list, which include Recessed LED Luminaries, CCTV Cameras/CCTV […]

The BIS CRS Certification for LED Luminaires for Road and Street lighting is certified under the (Compulsory Registration Scheme) Scheme II under Schedule II of the Bureau of Indian Standards (Conformity Assessment) Regulations, 2018. The certification process requires certain documents and procedures to be followed. BIS Regulation on Electronics and Information technology goods (Requirement of compulsory […]

The Ministry of Information and Technology passed an order on 16th March 2021 titled “Electronics and Information Technology Goods (Requirement of Compulsory Registration) Order, 2021.”  The order made it mandatory for the products specified in the schedule to carry a “Standard” mark under the Scheme II of Schedule II of the Bureau of Indian Standards […]

The BIS ISI Certification for Galvanized Steel Sheets are certified according to Indian Standards IS 277:2018. The Certification is made under Scheme-I of the Bureau of Indian Standards-(Conformity Assessment) Regulations, 2018, for Products, Including Galvanized Steel Sheets. There are a few tests to be conducted before the Certification is granted to the manufacturers of the […]

The Ministry of Health and Family Welfare issued a notification on 14th October 2022 in notification no. GSR 778 (E) informed about the amendment of the New Drugs and Clinical Trials (Third Amendment) Rules, 2022. The draft for the same amendment was notified vide notification no. GSR 32 (E ) dated 21st January 2022, which […]

The Department of Legal Metrology, Under the Government of Goa, issued a notification on 28th July 2022 notifying about the Goa Legal Metrology (Amendment) Rules, 2022, to amend the Goa Legal Metrology Rules, 2011. The draft rules “Goa legal Metrology (Amendment) Rules, 2022” for the same purpose were published on 28th April 2022 and have […]

The Ministry of Health & Family Welfare (MoHFW) issued GSR 754 (E) on 30th September 2022, notifying about the Medical Devices (Fifth Amendment) Rules, 2022. A Draft for the same was issued in notification number G.S.R. 104(E) on 9th February 2022, which has further been finalized as “Medical Devices (Fifth Amendment) Rules, 2022”. The Fifth […]

The Ministry of Health and Family Welfare or MoHFW notified G.S.R. 777 (E) on 14th October 2022, Notifying about the Medical Devices (Sixth Amendment) Rules, 2022. A draft for the same was issued in notification no. G.S.R. 710(E) on 20th September 2022, which this notification has further finalised as “Medical Devices (Sixth Amendment) Rules, 2022”. […]

Before 2006, the Medical Device Industry was utterly unregulated in India. Customers were exposed to various health and life threats caused by unregulated, cheap-quality medical devices. With the increase in the medical device industry, the risks increased. Due to customers’ exposure to unregulated medical devices, CDSCO mandated the registration of medical devices before being manufactured, […]

Before 2006, there was no such law governing the Medical Device Industry in India. The devices had no regulation or licenses, which exposed the consumers to health and life risks. Later, the Central Drug Standard Control Organization made it mandatory for all medical devices to be regulated before they were sold or marketed in India. […]

The Drugs Controller General of India, or DCGI, issued a notification on 16th March 2022, which notified about the classification of medical devices pertaining to CDSCO Registration for General Hospital Medical Devices under the provisions of Medical Device Rules, 2017. The notification includes 146 Medical Devices based on their Intended Use and Risk Classification. Overview […]