CDSCO classifies In-Vitro Diagnostic Medical Devices under Medical Device Rules, 2017

This classification has been undertaken on the basis of intended use, risk associated with the device and other parameters. CDSCO has updated its List of In-Vitro Diagnostic Medical Devices (IVD Analyzers) and List of In-Vitro Diagnostic Medical Devices (IVD Instruments). It has also added List of In-Vitro Diagnostic Medical Devices (IVD- Specimen receptacle) and List of In-Vitro Diagnostic Medical Devices under provisions of sub-rule (2) rule 4 of the Medical Devices Rules, 2017.

PCI directs State Councils to Implement Jan Vishwas Act, 2023

The Jan Vishwas Act has introduced a provision for adjudication of penalties under the Pharmacy Act. The provision empowers the central government to authorise the President of the State Council, where the alleged violation is committed, to be the adjudicating officer for holding an inquiry and impose penalty.

Union Health Minister addresses Gender Discrimination in India

The Union Minister for Health and Family Welfare, chaired the 29th meeting of the Central Supervisory Board (CSB). The central focus of the meeting was the concerning decline in the Child Sex Ratio (CSR) and Sex Ratio at Birth (SRB) in the country, highlighting the ongoing battle against sex-based discrimination and its consequences, including sex selection and pre-birth elimination.

Special campaign 3.0 of Department of Pharmaceuticals

Physical files numbering 3239 have been reviewed so far against 5539 physical files targeted for review. The review has helped weed out 820 files. Against 62 public grievances, cases pending at the start of campaign and included in target for clearance, 39 PG cases have already been addressed. The Department is still maintaining a NIL report as regards Public Grievances Appeals are concerned.

Efficiency Measures Implemented for Document Submission to CDSCO

These measures are designed to expedite the processing of documents within the CDSCO, reducing paperwork and enhancing the overall efficiency of regulatory affairs. The move towards digital documentation aligns with the broader global trend of modernizing administrative processes and promoting sustainable practices.