WHO to Include Ayurveda, Siddha, Unani Morbidity Codes

The ICD series by WHO serves as a global standard for classifying diseases, providing a common language for health information. While the existing data primarily reflects modern biomedical practices, the upcoming ICD 11 TM Module 2 aims to incorporate data and terminology from Ayurveda, Siddha, and Unani (ASU) systems, bringing global uniformity to the classification of traditional medicine.

New Drug Manufacturing Rules Introduced to Strengthen Quality Standards

The Amendment Rules introduce a new set of guidelines titled “GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS” in Schedule M. The guidelines outline several key principles to be adhered to by pharmaceutical manufacturers, focusing on pharmaceutical quality systems, quality risk management, sanitation and hygiene, qualification and validation, complaints and adverse reactions, product recalls, and change control.

Union Health Minister Inaugurates CDSCO Sub Zonal office & CDTL in Indore

The Central Drug Testing Laboratory, equipped with high-quality laboratory services, will play a crucial role in testing drugs, ensuring the availability of essential and high-quality medicines to improve the health of citizens. The facility is equipped with advanced instruments, including 12 HPLCs, 1 GLC, and 1 UV Spectrophotometer.

NPPA sets Retail Prices for 19 Formulations

Manufacturers of specific formulations categorized as “new drugs” under the Drug Price Control Order (DPCO), 2013 (DPCO, 2013) are required to set the retail price as indicated in this notification. Manufacturers can add Goods and Services Tax to the retail price only if they have already paid or are liable to pay the government on the mentioned retail price. Manufacturers must issue a price list in Form–V via IPDMS to the National Pharmaceutical Pricing Authority (NPPA) and submit copies to State Drug Controllers and dealers.

Blood Centres Can Only Charge Processing Charges For Blood

The Central Drugs Standards Control Organisation (CDSCO) has issued an advisory requiring adherence to the Revised Guidelines- 2022 for Recovery of Processing Charges for Blood and Blood Components issued by NBTC. The advisory states that during the Drugs Consultative Committee meeting it was opined that blood is not for sale and hence the blood centres shall charge only processing costs.

Over 1 Crore Screened for Sickle Cell Disease under National Sickle Cell Anaemia Elimination Mission

The National Sickle Cell Anaemia Elimination Mission operates in a mission mode, focusing on screening, prevention, and management of sickle cell anemia in all tribal and high-prevalence areas across states and union territories in India. The Ministry aims to build on this momentum, continuing its efforts to reach the set target of screening 7 crore people within the stipulated three-year period.

CDSCO Launches National Single Window System Portal

This portal has been designed to build a system that functions as a one-stop shop for all the approvals required by the investor and facilitates ease of doing business. The NSWS Portal for CDSCO will be independent of the SUGAM Portal or the cdscomdonline portal.

Clarification on Approval Process for TAVI/TAVR and IVL Procedures under CGHS

The OM reiterates that the approval from the Director, CGHS, in consultation with the Special Technical Committee (STC) is needed for Transcatheter Aortic Valve Implantation/Replacement (TAVI/TAVR) and Coronary Intra Vascular Lithotripsy (IVL) or Shock Wave Lithotripsy procedures under CGHS. This clarification aims to streamline the process of obtaining approval for TAVI/TAVR and IVL procedures, ensuring that the highest standards of patient care are maintained under the CGHS.