DEPARTMENT OF TRADE & TAXES
GOVT. OF NCT OF DELHI
VYAPAR BHAWAN,IP ESTATE, NEW DELHI

PUBLIC NOTICE

Attention of the persons registered, under DGST/CGST Act is hereby drawn to Rule 18 of Delhi Goods and Services Tax Rules, whereby, it is mandatory to display the certificate of registration at a prominent location at principal place and  every additional place or places of business.

It is also mandatory to display Goods and Services ‘ Tax Identification Number (GSTIN) on the name board exhibited at the entry of the principal place of business and at every additional place of business.

Violation of the above provisions of the Act my attract penalty upto Rs. 25000/- u/s 125 of re DGST Act. This penalty is leviable under CGST Act also separately.

Therefore, all registered persons are hereby advised to ensure that Rule 18 of DGST Rules is complied by them.

DIP/Shabdarth/0324/20-21

Commissioner
Delhi State

To be published in the Gazette of India Extraordinary Part II Section 3, Sub Section (II)

Government of India
Ministry of Commerce & Industry
Department of Commerce
Udyog Bhawan, New Delhi

Notification No: 19 /2015-2020
New Delhi, the (17th August, 2021)

Subject: Scheme Guidelines for Remission of Duties and Taxes on Exported Products (RoDTEP)

S.O.(E): In exercise of the powers conferred by Section 5 of the Foreign Trade (Development and Regulation) Act, 1992 read with Para 1.02 of the Foreign Trade Policy 2015-20, the Central Government hereby makes the following amendments in the Foreign Trade Policy 2015-20 with immediate effect:

APPENDIX 4R : Scheme for Remission of Duties and Taxes on Exported Products (RoDTEP)

30th September, 2021 is last date for voluntary registration of Manufacturers for their Medical Devices made in India at CDSCO https://cdscomdonline.gov.in/NewMedDev/Homepage.

Please register if not done or inform reasons / challenges/ inability for not doing so and help desired.

After 30th September, 2021 Medical Devices that are not registered will not be permissible to manufacture, import or sell in India without prior compulsory registration.

Dear Members,

Due to the Security reasons on the occasion of Independence Day, it is requested that all the shops & establishments shall remain closed on 14th August 2021 in the vicinity of Bhagirath Palace & Chandni Chowk.

Regards

Puneet Bhasin
Secretary -SMTA

DATE: 9th August 2021

To be published in the Gazette of India Extraordinary Part-II, Section-3, Sub-Section (II)

Government of India
Ministry of Commerce & Industry
Department of Commerce
Directorate General of Foreign Trade

Notification No.16, 2015-2020
New Delhi, Dated: 9th August, 2021

Subject: Extension in period of modification of IEC till 31.08.2021 and waiver of fees for IEC updation done during August, 2021— reg.

S.O.(E): In exercise of powers conferred by Section 3 read with Section 5 of FT (D&R) Act, 1992, read with paragraph 1.02 and 2.01 of the Foreign Trade Policy, 2015-2020, as amended from time to time, the Central Government hereby amends the provision in Para 2.05(d) of Chapter-2 of Foreign Trade Policy, 2015-2020 as under:

DATE: 30th July 2021

File No.-20(8)/43/2021/Div.VI/NPPA
Government of India
Ministry of Chemicals & Fertilizers
Department of Pharmaceuticals
National Pharmaceutical Pricing Authority

OFFICE MEMORANDUM

The Government vide Gazette Notification No. S.O. 2899(E) dated 20^th July 2021 has made an amendment in the Drugs (Prices Control) Order, 2013 by inclusion of Form-VI “Proforma for Price List of Medical Devices”. The same is enclosed for your reference as Annexure-I.

DATE: 23rd July 2021

Drugs Controller General (India)

Directorate General of Health Services
FDA Bhawan, Kotla Road, New Delhi

NOTICE

File No. IVD/Misc/196/2020

Subject: Classification of In-vitro Diagnostic Medical Devices under the provisions of Medical Devices Rules, 2017 – Regarding.

Safety, quality and performance of Medical Devices and In-vitro Diagnostic Medical Devices are regulated under the provisions of the Drugs and Cosmetics Act, 1940 and rules, made there under. For the regulation of Medical Devices and In-vitro Diagnostic Medical Devices with respect to the import, manufacture, clinical investigation, clinical performance evaluation, sale and distribution, the Central Government, after consultation with the Drugs Technical Advisory Board, has notified Medical Devices Rules, 2017 vide G.S.R. 78(E) dated 31.01.2017 which is already implemented from 01.01.2018.

DATE: 26th July 2021

Drugs Controller General (India)
Directorate General of Health Services
FDA Bhawan, Kotla Road, New Delhi

Notice

File No. 29/Misc./0312020-DC (147) 

Subject: Classification of Medical Device pertaining to Dermatological & Plastic Surgery under the provisions of Medical Devices Rules, 2017- Reg.

Safety, quality and performance of medical devices are regulated under the provisions of the Drugs and Cosmetics Act, 1940 and rules made thereunder. For the regulation of medical devices with respect to the import, manufacture, sale and distribution, clinical investigation, the Central Government, after consultation with the Drugs Technical Advisory Board, has notified Medical Devices Rules, 2017 vide G.S.R. 78 (F) dated 31.01.2017 which is already implemented from 01.01.2018

DATE: 26th July 2021

Drugs Controller General (India)
Directorate General of Health Services
FDA Bhawan, Kotla Road, New Delhi

Notice

File No. 29/Misc./03/2020-DC (202)

Subject: Classification of Medical Device pertaining to Physical support under the provisions of Medical Devices Rules, 2017- Reg.

Safety, quality and performance of medical devices are regulated under the provisions of the Drugs and Cosmetics Act, 1940 and rules made thereunder. For the regulation of medical devices with respect to the import, manufacture, sale and distribution, clinical investigation, the Central Government, after consultation with the Drugs Technical Advisory Board, has notified Medical Devices Rules, 2017 vide G.S.R. 78 (F) dated 31.01.2017 which is already implemented from 01.01.2018