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

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):

APPENDIX 4 R – Notified on 17-08-2021 under Notification No 19/2015-20

APPENDIX 4R : Scheme for Remission of Duties and Taxes on Exported Products (RoDTEP) RODTEP Entry No. Tariff Item Description of Goods (As per CTH ) RODTEP Rate as % age of FOB (#) UQC Cap (Rs. Per UQC) (1) (2) (3) (4) (5) (6) 0301 LIVE FISH Ornamental Fish 1 03011100 Freshwater 0.5% Kg

Last date for voluntary registration of Manufacturers

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,

All the shops & establishments shall remain closed on 14th August 2021

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  

Extension in period of modification of IEC

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

Office Memorandum Dated 30th July 2021

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 20th July 2021 has made an amendment in the Drugs (Prices Control) Order, 2013 by inclusion of Form-VI “Proforma for Price List of Medical

No. SMTA/JULY-31/Prayer Meeting

No. SMTA/July.31/Prayer Meet With profound grief & sorrow, we regret to inform the sad demise of our beloved Smt Chander Prabha Sareen W/o Late Sh. Suraj Prakash Sareen on 21st July 2021. Rasam Pagdi will be held on 31st July 2021, Saturday from 3:00 PM to 4:00 PM at Ashoka Bhawan, Ashoka Niketan, Anand Vihar,

Classification of In-vitro Diagnostic Medical Devices

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

Classification of Medical Device pertaining to Dermatological & Plastic Surgery

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

Classification of Medical Device pertaining to Physical support

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