Snehita Shukla

About Snehita Shukla

Snehita has her qualifications in B.Com LLB and LLM, and holds a specialization in Corporate & Financial Laws and Policy. She is hardworking, dedicated and sincere. She has a great command in english and has great problem solving, critical thinking and writing skills which makes her stand out of the crowd. She has a keen interest in legal research work and content writing, she also has a hold in legal research methodology. She loves to take challenges and to explore new topics to research on. She aims to improve her knowledge and skills through her experience.

BIS CRS Certification for USB Type External HDD

The Ministry of Electronics and Information technology issued a notification on 1st April 2020, notifying about the addition of product categories to the schedule of the “Electronics and Information Technology Goods (Requirements for Compulsory Registration) Order, 2012” under the Compulsory Registration Scheme (BIS CRS). The Central Government has included 12 new electronic products under the […]

Trademark Dispute between Varun Gems vs. Precious Jewels and Ors. – A Complete Analysis

The case of Varun Gems vs. Precious Jewels and Ors. was an outcome of the infringement of legal rights obtained by a registered trademark under the Trademarks Act 1999. The case brought into question the use of the term “bona fide”, as mentioned in section 35 of the Trade Marks Act, 1999. The order of […]

BIS Notification Regarding Date of Establishment and Withdrawal of Certain Indian Standards

The BIS, under the Department of Consumer Affairs, issued a notification in an Official Gazette on 11th October 2022. The Notification was published with regard to the Date of Establishment and Withdrawal of Certain Indian Standards in India. The BIS notified about certain Indian standards established by BIS on certain dates and also informed about […]

CDSCO Medical Device Registration for Paediatrics and Neonatology

The Central Drug Standard Control Organization, or CDSCO, is the national regulatory authority of India, headed by the DCGI. The Medical Device Rules, 2017, were introduced to regulate the laws and rules related to the Manufacture, Import, Clinical Investigation, Distribution and Sale of Medical devices in India. On 23rd August 2021, the DCGI notified CDSCO […]

CDSCO Registration for Respiratory Medical Device- A complete analysis

Medical device safety, quality, and performance standards are governed by the Drugs and Cosmetics Act of 1940 and the rules promulgated thereunder. The Drugs Controller General of India under the Directorate General of Health Services notified on 6th August 2021, under the Medical Device Rules of 2017, regarding the CDSCO Registration for Respiratory Medical Devices. […]

Flavoured Tea Registration – How to Apply?

According to Notification GSR 694(E), which was issued on 11th October 1999, no person can carry on the activities of manufacturing tea with added flavour without obtaining a Flavoured Tea Registration from the Tea Board as a bonafide manufacturer of flavoured tea, according to the order in respect of each factory owned or controlled by […]

Trademark Registration for Pharmaceutical Products – An Analysis

The industry with the fastest growth in India is pharmaceuticals. India exports about 20% of the pharmaceutical products sold worldwide. India is a source of organic and inorganic pharmaceutical products for various global economies. However, it is also true that Pharma Companies face intense competition in the drug industry and that their costs for branding […]

BIS Standards for Lead Acid Batteries – An Overview

In May 2019, the Standards and Quality Control Division of the Ministry of New and Renewable Energy published a notice announcing the introduction of mandatory BIS certification for solar PV modules, inverters, storage batteries, etc. The notification clarified that the Indian Standards IS-16270: 2014’s Storage Battery standards would apply to the BIS Standards for Lead […]

Start a Profitable Coir Business in India: Requirements and Licenses

More than two-thirds of the globally marketed coir and coir-related products are produced in India. India does have a long coastline covered in coconut palms. Still, significant coconut-growing regions and Territories like Karnataka, Orissa, Maharashtra, Andaman & Nicobar, Pondicherry, Tamil Nadu, Goa, Lakshadweep, Kerala, Assam, and others are where the coir business or industry is […]

CDSCO Registration for Rheumatology Medical Devices

The Central Drug Standard Control Organisation issued a notice on 3rd September 2020, which notified about the classification of Non-notified Medical Devices and their registration under CDSCO. The notification listed the category 24 non-notified medical devices as per the classification in the first schedule of Medical device rules, 2017. The list also includes a classification […]

CDSCO Medical Device Registration for Pacemaker: Complete Guide

The DCGI issued a notice on July 26th 2021, stating the classification of medical devices pertaining to cardiovascular devices, per the provisions of medical device rules 2017. According to the classification, 36 non-notified devices be regulated as medical devices for the treatment of cardiovascular problems under the Medical Device Rules, 2017. The regulatory authorities have […]

CDSCO Registration for Dermatology and Plastic Surgery Medical Devices

The Drugs Controller General of India (DCGI) issued a notice S.O. 648 (E) & GSR 102 (E) on 26th July 2021, regarding the classification of medical devices related to Dermatological and Plastic Surgery, according to the provisions of Medical Device Rules, 2017. The regulatory authorities have also mandated CDSCO Registration for Dermatology and Plastic Surgery […]

How to Obtain AD Code for Export?

Authorised Dealer Code is a 14-digit numerical code given to an export business that has a current account with a bank. An AD Code must be registered at each port where customs clear the exporter’s goods. The AD Code for export for a specific port is necessary for customs clearance and must be provided to […]

Licensing Authorities for Medical Device Product Registration in India

In older times, manufacturing devices were sold without any law guiding them in India. In the year 2016, a rule was set forth which stated that the medical devices in India must be in accordance with the Medical Device Regulations, which are governed by Central Drug Standard Control Organization CDSCO. The CDSCO is the main […]