CDSCO classifies medical devices pertaining to operation theatre under the provisions of Medical Devices Rules, 2017.
These medical devices are classified into risk classes of A, B and C based on the intended use, risk associated with the device, and other parameters as specified under the medical device rules 2017.
RBI notifies Application form for Aadhar e-KYC Authentication License
In terms of Section 11A of the Prevention of Money Laundering Act (PMLA), 2002, the government through a notification may permit entities other than banking firms to authenticate client’s Aadhaar number using the e-KYC facility provided by the Unique Identification Authority of India (UIDAI). However, the notification shall be issued only after consulting with the UIDAI and the appropriate regulator.
Government of West Bengal Grants paid holiday to employees on the occasion of Assembly elections.
The Daily wage/casual workers are also entitled for a holiday and wages on poll day as provided in Section 135B of the Representation of Peoples Act, 1951.
CDSCO classifies medical devices pertaining to Personal Protective Equipment.
The General intended use given against each of the devices is for guidance to the applicants intend to furnish application of import or manufacture of medical devices under the provisions of Medical Devices Rules, 2017. However, a device may have specific intended use as specified by its manufacturer.
CDSCO has Classified Medical Devices Pertaining to General hospital.
The Drug Controller General has classified 57medical devices related to General Hospital which includes Electrically powered spinal fluid pressure monitor, Apgar timer, Clinical color change thermometer, Manual adjustable hospital bed, Medical bassinet etc.
CDSCO classifies medical devices pertaining to Nephrology and Renal care under the provisions of Medical Devices Rules, 2017.
These medical devices are classified into risk classes of A, B and C based on the intended use, risk associated with device and other parameters as specified under the medical device rules 2017.
DGFT clarifies procedure for refund of application fees deposited by applicants for Restricted Import Authorization for Moong, Tur and Urad
Applicants are requested to withdraw their restricted import authorization application after logging onto the DGFT Website.
After withdrawal of application, request for refund is to be made at the DGFT Website.
FSSAI operationalises provisions of FSS(Food Products Standards and Food Additives) Amendment Regulations, 2021 relating to limit of naturally occurring formaldehyde in freshwater and marine fish
Meanwhile the provisions specifying the limit of naturally occurring formaldehyde in freshwater and marine fish is being reoperationalised. The Food Business Operators shall follow these regulations and the enforcement of these regulations with immediate effect.
Assam PCB has provided clarification regarding issue of provisional consent to establish ethanol producing industries
In case the project proponent is unable to submit any necessary documents along with application for provisional consent, they shall submit self attested declaration to guarantee that they shall submit the necessary documents within 30 days from issue of provisional consent to establish.
