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NPPA asks manufacturers to submit data on certain dosage forms of nicotine to fix ceiling prices
The National Pharmaceutical Pricing Authority (NPPA) has called for data from the manufacturers of specific forms of scheduled formulations of nicotine, used for nicotine Read more...
Indian pharma hopes for policy-level clarifications & simplifying APA procedures in Union Budget 2025
Indian pharmaceutical industry, which is a significant contributor to the country’s economy, has outlined its expectations for the Union Budget 2025 which will be present Read more...
FIEO to host power talk ‘SME in Focus’ for SMEs in pharma sector in Hyderabad on January 24
The Federation of Indian Export Organisations (FIEO), in collaboration with the Pharmaceuticals Export Promotion Council of India (Pharmexcil), the Bulk Drug Manufacturer Read more...
Drug supply to entire north east may collapse if more time is not given to comply with revised Schedule M: ASSPMA
The Assam Small Scale Pharmaceutical Manufacturers Association (ASSPMA) has informed the Union health ministry that if the pharma manufacturing units in Guwahati are not Read more...
DGFT notifies updated export policy aligned with Finance Act 2024 to boost pharma trade efficiency
In a major step to align India’s pharma export regulations with global standards, the Directorate General of Foreign Trade (DGFT) has officially notified the updated Sche Read more...
PDMA asks govt to create separate category for units below Rs. 10 crore & allow 3 years to implement revised Schedule M
The Punjab Drug Manufacturers Association (PDMA) has sought the Union ministry of health and family welfare to create a separate category for units below Rs. 10 crore tur Read more...
FOPE urges govt to extend revised Schedule M implementation to December 31, 2026
The Federation of Pharmaceutical Entrepreneurs (FOPE), which has welcomed the extension of the revised Schedule M implementation to December 31, 2025, has now noted pract Read more...
HPMA demands three years’ time for full compliance with revised Schedule M
The Haryana Pharmaceutical Manufacturers Association (HPMA) has demanded to the Union health ministry to allow three years to upgrade their manufacturing plants to the st Read more...
India initiates anti-dumping probe on Resorcinol imports from China and Japan
The Directorate General of Trade Remedies (DGTR) has issued an updated notification concerning the ongoing anti-dumping investigation into imports of Resorcinol from Chin Read more...
MP DCA forms team of regulatory officers to assist pharma units in upgrading plants as per revised Schedule M
The drug control administration under the Food and Drug Administration in Madhya Pradesh has formed one team of regulatory officers to provide support and guidance to the Read more...
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