TOP 5 HEALTH LAWS AND POLICY UPDATES

Dear Readers, we are happy to share the most interesting legal and policy updates concerning health industry that we read today. We hope you enjoy reading it.

1. India’s Department of Consumer Affairs has requested comments from stakeholders regarding the declaration of units of measurement for the net quantity of food wrapping paper and aluminum foils used for carrying food products. The proposal suggests including both “weight” and dimensions (length x breadth), i.e., kg and meters x meters (or cm x cm), rather than only weight or dimensions. This proposal aims to inform consumers about the actual quantity of packing material delivered.
Source: bit.ly/3Yld47H

2. The Indian Pharmacopoeia Commission (IPC), under India’s Health Ministry, has released an updated Medical Device Adverse Event Reporting Form for the reporting of Medical Device Adverse Events (MDAEs). The form states that reporting any MDAE will not have any legal implications for the reporter, and the reporter’s identity will be protected and kept strictly confidential.
Source: bit.ly/3XYGbwc

3. India’s Ministry of Health and Family Welfare (MoH&FW) is considering a proposal to amend the timelines for conducting audits and verifying compliance for grant of manufacturing license for medical devices in India. Currently, the Medical Devices Rules, 2017, do not specify these timelines, leading to delays in Quality Management System (QMS) inspections and the subsequent compliance verification processes.
Source: bit.ly/3ZXbr12

4. India’s Ministry of Health and Family Welfare (MoH&FW) is considering a proposal to restrict the eligibility requirements for qualifying as a competent person for obtaining a wholesale license for the sale, stocking, exhibition, or distribution of drugs in India to those with a pharmacy background, specifically D. Pharmacy, B. Pharmacy, M. Pharmacy, Pharm D, or individuals who are Registered Pharmacists.
Source: bit.ly/3ZXbr12

5. The Ministry of Health and Family Welfare (MoH&FW) is considering a proposal to ensure mandatory reporting of Serious Adverse Events (SAE) related to medical devices, including In-Vitro Diagnostic Medical Devices, by the manufacturer or importer of these devices in India. Currently, under the Medical Devices Rules 2017, there is no mandatory requirement for reporting such events by the license holder.
Source: bit.ly/3ZXbr12

TOP 5 HEALTH LAWS AND POLICY UPDATES

Dear Reader, we are happy to share the most interesting legal and policy updates concerning health industry that we read today. We hope you enjoy reading it.

1. India’s Environment Ministry has proposed to introduce extended producers responsibility for scrap of non-ferrous metals by way of amendment to Hazardous and Other Wastes (Management and Transboundary Movement) Second Amendment Rules, 2016.
Source: bit.ly/4fQHG7E

2. The deadline for declaration and registration of exotic animal species in possession of various individuals, organizations, zoos, etc is 28th August 2024. The registration of these exotic animal species is to be done in the PARIVESH 2.0 portal.
Source: bit.ly/3XaaXTA

3. India’s apex telecom regulator, the Telecom Regulatory Authority of India (“TRAI”) has issued directions to curb misuse of messaging services and protect consumers from fraudulent practices. TRAI has mandated that the messages containing URLs/ APKs/ OTT links/ Call back numbers, which are not whitelisted will not be sent with effect from 1st September 2024.
Source: bit.ly/3Xeorhb

4. A Texas Court has stayed the operation of ban on non-compete agreements stating that the Federal Trade Commission (FTC) lacks the authority to ban non-compete agreements which was supposed to go into effect 4th September 2024.
Source: bit.ly/3SYlZsy

5. The Supreme Court of India, while observing the working conditions of doctors and healthcare professionals and their susceptibility to violence, has constituted a ten (10) member task force to formulate a national framework (protocol) for ensuring their safety and facilities. The task force will submit its interim report within three (3) weeks and final report within two (2) months.
Source: bit.ly/4cHpv1C