NMC notifies Draft National Medical Commission Registered Medical Practitioner (Professional Conduct) Regulations, 2022.

As per the draft regulation, the registered medical practitioner (RMP) should attend continuing professional development programs regularly each year, totaling at least 30 credit hours every five years. Only recognized medical colleges and health institutions or medical societies accredited or authorized by EMRB/State medical Councils can offer training and credit hours for this purpose.

Government of Telangana notifies amendments to Telangana State Factories Rules.

No person shall carry out any demolition of plants or structures containing friable asbestos insulation material and removal of asbestos from building or structures in which asbestos is liable to become air-borne, unless he is recognized and duly empowered by the Chief Inspector of Factories as qualified to carry out such work in accordance with the provisions of this Schedule.

SEBI modifies cyber security and cyber resilience framework of stock exchange, clearing corporation and depositories.

MIIs should carry out periodic vulnerability assessment and penetration testing (VAPT) which inter-alia includes all critical assets and infrastructure components like Servers, Networking systems, Security devices, load balancers, other IT systems pertaining to the activities done as a role of MII etc., in order to detect security vulnerabilities in the IT environment and in-depth evaluation of the security posture of the system through simulations of actual attacks on its systems and networks.

Revised policy for import of Oxytocin

Import of Oxytocin reference standards falling under
HS Codes 29371900, 29372900, 29379019, 29379090 and all HS Codes at 8 digit level under 3004 is permitted exclusively for the purpose of test and analysis subject to submission of Test License issued by the DGCI / CDCSO.

Draft Drugs (Amendment) Rules, 2022

Where an application is made for the manufacture of drug formulation falling under the purview of New Drug as per the New Drugs and Clinical Trials Rules, 2019 or Drugs Rules, 1945, as the case may be, the license to manufacture for sale or distribution of the drugs shall be granted after approval of the drug as new drug.