Snehita Shukla

Chapter V of the Medical Device Rules 2017[1] covers rules and regulations for importing Medical Devices into India. It discusses the conditions and rules for grant of Import licenses for multiple purposes. It allows Import of Medical Device for Personal Usein small quantity, which are otherwise prohibited for import as per section 10 of The […]

The Indian government’s Central Drugs Standard Control Organisation (CDSCO) is in charge of issuing import licences for cosmetics. For a cosmetic product to be imported into India for marketing purposes, the applicant or manufacturer must fill out form COS-2. First, the applicant must sign up on the Sugam online portal. After signing up, users should […]

There has been a huge expansion of the cosmetic market in India, with a huge range of Korean beauty and cosmetic products. India has been a great attraction for businesses trying to expand their market, especially after the introduction of the online marketing system. The online selling culture has increased the scope of online marketing […]

CCTV cameras are most commonly used these days for the purpose of safety and security at home, offices, schools, hospitals, public places etc. The widely used product, with its technology, has helped people from all over the world to monitor and control safety and security throughout the year. CCTV cameras are of major use in […]

A smartwatch is a fashion statement these days. The features it has are useful for almost every daily activity we do. From keeping track of the sleep cycle to noting down the stress level of the body, the smartwatch technology has most of the features that help in keeping a check on the current lifestyle […]

The Central Drugs Standard Control Organisation (CDSCO) operates under the Directorate General of Health Services, the Ministry of Health & Family Welfare, under the Indian government. It is the National Regulatory Authority (NRA) of India. The Drugs and Cosmetics Act of 1940[1] now requires the registration of all medical devices as of April 1, 2020, in addition […]

The Central Drugs Standard Control Organisation is the highest Indian regulatory body that oversees the production of medical devices that have been approved (CDCSO). In India, the regulatory authority is in charge of licencing and approving the production of medical devices. FORM MD-7 and FORM MD-9 are used by this regulatory agency to issue manufacturing licences, […]

It is mandatory for pressure cookers to get BIS certification as per Indian Standards IS 2347. BIS ISI for pressure cookers has been mandated by the Bureau of Indian Standards, which is the National Standard Body of India, and was established under the BIS Act 2016[1]. The BIS, under the gazette of India, has set […]

Aluminium foil is the most common product used in every household kitchen for the purpose of food packaging and storing. As it is utilized by the common public to store and pack their everyday food items, it is important that the foil does not emit any harmful substance in the food. For this purpose, it […]

The Drugs and Cosmetics Acts, 1940 and The Drugs and Cosmetics Rules, 1945[1] are the two laws governing the Import, sales, manufacture and distribution of Drugs in India. Any product falling under the category of Drugs or Medical related devices needs to be registered before getting imported to India. It is also required to register […]

As per the standards of BIS ISI, it is mandatory for all Electric immersion water heaters to be certified as per IS Standard: IS 368:2014. According to the standards of BIS ISI for water heaters, it is mandatory to get them certified as per IS Standard- IS 368:2014. Without getting certified by BIS ISI, the […]

It is mandatory to get BIS ISI for Mixer/Juicer as per standards IS 302 part 2 section 14 and IS 4250 by BIS. It is mandatory to obtain BIS ISI for Mixer/Juicer, also known as domestic electric food mixer and centrifugal Juicer, as per IS standards IS 4250. IS 302 part 2, Section 14 is […]

During any Import or Export, if any Importing or Exporting good contains medical-related products, then such goods need to obtain no objection certificate (NOC) from the Drug controller office of government, or any such competent body, which is authorized to manufacture those medical-related products. No Objection Certificate is an approval given to the Manufacturer of […]

According to the Medical Devices Rules of 2017[1], any business seeking a loan licence to produce Class A or Class B medical devices must submit an application. In vitro diagnostic devices may also be categorised as Class A or Class B medical devices because they are low and low-to-moderate risk devices. The manufacturer must submit […]