Updated on : 07-07-2025
| The Minimum Requirements for Biological Products will be amended as follows:Regarding the article of “Inactivation test” in the section of “Tests on final product” of the monograph for “High dose Influenza HA Vaccine”, the rule of inoculating with the allantoic fluid into allantoic cavities of eggs in case there are positive hemagglutination test results will be partially amended. And regarding the standard for “Pneumococcal Polyvalent Vaccine”, the section of “Serological identification test” will be deleted. In addition, the standard for “21-valent Pneumococcal Conjugate Vaccine” that is to be newly approved will be added.The Public Notice on National Release Testing will be amended as follows: The criterion, fee, quantity and Institution for National Release Testing for “21-valent Pneumococcal Conjugate Vaccine” that is to be newly approved will be added. |
| Title | Category | Created On |
|---|---|---|
| National Enquiry Point (NEP) Guideline 2025 | Administrative Ruling | 2025-11-04 09:35:43 |
| Ukraine: Draft Resolution of the Cabinet of Ministers of Ukraine "On Amendments to Resolutions of the Cabinet of Ministers of Ukraine No. 539 of 10 May 2024 and No. 847 of 23 July 2024" | TBT | 2025-11-02 05:27:46 |
| Ukraine: Draft Resolution of the Cabinet of Ministers of Ukraine “On Amendments to Resolution of the Cabinet of Ministers of Ukraine No. 376 of May 26, 2005” | TBT | 2025-11-02 05:25:38 |
| Saudi Arabia: The Kingdom of Saudi Arabia/ Honey | SPS | 2025-11-02 05:21:45 |
| Saudi Arabia: Transportation of public health pesticide | SPS | 2025-11-02 05:07:11 |