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Therapeutic Goods Legislation Amendment (Australian Unique Device Identification Database and Other Measures) Regulations 2025 1, the Honourable Sam Mostyn AC, Govemor-General of the Commonwealth of Australia, acting with the advice of the Federal Executive Council, make
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In the pharmaceutical and healthcare industries, Qualification and Validation are essential to ensure that facilities, systems, and processes consistently produce the desired results. Following Good Practice (GxP) guidelines ensures compliance with regulatory standards like WHO, USFDA,
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INTERNATIONAL COUNCIL FOR HARMONISATION OF TECHNICAL REQUIREMENTS FOR PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED GUIDELINE STABILITY TESTING OF DRUG SUBSTANCES AND DRUG PRODUCTS Q1 Draft version Endorsed on 11 April 2025 Currently under public consultation At
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File No. 4-01/2023-DC (Misc. 3)Government of IndiaDirectorate General of Health Services Central Drugs Standard Control Organization(FDC Division) FDA Bhawan, Kotla RoadNew Delhi-110002Dated: 11 April 2025 To,All State/ UT’s Drugs ControllersSubject: Manufacturing and marketing of unapproved FDC’s
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GJ/AHD/C-05369 GOVERMENT OF GUJARAT LICENSE TO ELECTRICAL CONTRACTORS Authorized by Govt. Notification, E & P Deptt., No. GU/2013/37/ELA/11-2012/2401/K, Dated 22.04.2013 M/s.QXP PHARMA PROJECT and GMP SERVICES PRIVATE LIMITED, Dist-AHMEDABAD is hereby authorized to carry out Electrical
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MINISTRY OF HEALTH AND FAMILY WELFARE (Department of Health and Family Welfare) NOTIFICATION New Delhi, the 4th January, 2025 G.S.R. 10(E).—Whereas the Drugs Rules, 1945, were amended and published as required under sub-section (1) of section
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