MoHFW appoints 25th January 2022 as the date on which the provisions of Assisted Reproductive Technology (Regulation) ACT , 2021 shall come into force.

The Assisted Reproductive Technology (Regulation) Act, 2021 is for regulating and supervising the assisted reproductive technology clinics and the assisted reproductive technology banks, and prevention of misuse.

MoHFW appoints 25th January 2022 as the date on which the provisions of Surrogacy (Regulation) ACT , 2021 shall come into force.

The Act prohibits commercial surrogacy and allows only altruistic surrogacy which involves no monetary compensation to the surrogate mother other than the medical expenses and insurance coverage during pregnancy.

New Drugs and Clinical Trials (2nd Amendment) Rules, 2022

The authority designated by the Central Government in the Ministry of Health and Family Welfare, Department of Health Research under these rules shall act an registration authority under the act for the purpose of registration …

Drugs (2nd Amendment) Rules, 2022

Liquid Antiseptics for household use is exempted from requirement of sale license in Form 20 or Form 20A.

The Drugs (Amendment) Rules, 2022.

As per the amendment under rule 96(5) every active pharmaceutical ingredient (bulk drug) manufactured or imported in India shall bear Quick Response code on its label at each level packaging that store data or information …

The Medical Devices (Draft Amendment) Rules, 2021.

If the manufacturer or licensee fails to comply with any of the conditions of an import license, or any provisions of the Act and these rules, the Central Licensing Authority may after giving the manufacturer …

Medical Devices (Amendment) Rules, 2022

The amendment provides that a provisional registration number shall be generated which will remain valid up to the 31st May, 2022 if the applicant submits, on or before the 28th February, 2022, an undertaking that …

New Drugs and Clinical Trials (Amendment) Rules, 2022

The amendment has extended the scope of new drugs to include cell or stem cell derived product. Previously the definition of new drug under the New Drugs and Clinical Trials Rules only included stem cell …

PCI Introduces late fee in respect of institutions which have failed to apply on PCI portal during approval process 2022-2023.

The Institutions which have forgotten the user ID& Password are required to submit the duly notarized affidavit on 100 rupees court paper in the prescribed format so as to reach the council’s office on or …

DCI issues advisory on providing Dental Treatment.

The dental treatment shall be given to the patient by the registered dentist in his/her clinic/hospital.

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