Report Of A Series Of Expert Meetings On Developing Who Global Sodium Benchmarks November 2020 April 2021
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Report Of A Series Of Expert Meetings On Developing Who Global Sodium Benchmarks November 2020 April 2021
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Author : World Health Organization
language : en
Publisher: World Health Organization
Release Date : 2023-11-01
Report Of A Series Of Expert Meetings On Developing Who Global Sodium Benchmarks November 2020 April 2021 written by World Health Organization and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2023-11-01 with Medical categories.
In order to help drive progress towards the global target to reduce mean population sodium intake by 30% by 2025 for the prevention and control of NCDs, the World Health Organization (WHO) set global benchmarks for sodium levels in foods across different food categories, building on country experience of salt reduction. This is a report of a series of expert meetings, which WHO convened in November 2020, January 2021 and March 2021. The meetings were held virtually to review the results of the analyses of the existing country data on sodium targets; to assess priority food categories for which global sodium benchmarks should be developed; and to assess and finalize global sodium benchmarks for identified priority food categories.
Who Global Sodium Benchmarks For Different Food Categories
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Author : World Health Organization
language : en
Publisher: World Health Organization
Release Date : 2024-04-17
Who Global Sodium Benchmarks For Different Food Categories written by World Health Organization and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2024-04-17 with Medical categories.
The World Health Organization (WHO) has established the second edition of the global benchmarks for sodium levels in 70 food subcategories as part of WHO’s efforts in reducing the sodium intakes in populations. This is an updated edition of the first edition which was released in May 2021. The setting of global sodium benchmarks is a very important step to facilitate reformulation of food products which contributes to driving progress in sodium reduction. These global benchmarks are intended to be complementary to ongoing national and regional efforts to set sodium targets. Global sodium benchmarks are also intended to be useful for countries in setting national policies and strategies and for the ongoing dialogue between WHO and the private sector at the global level.
Technical Consultation On Setting Global Sodium Benchmarks For Different Food Categories
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Author :
language : en
Publisher: World Health Organization
Release Date : 2022-04-19
Technical Consultation On Setting Global Sodium Benchmarks For Different Food Categories written by and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2022-04-19 with Medical categories.
Who Global Sodium Benchmarks For Different Food Categories
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Author :
language : en
Publisher: World Health Organization
Release Date : 2021-05-03
Who Global Sodium Benchmarks For Different Food Categories written by and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-05-03 with Medical categories.
Who Expert Advisory Committee On Developing Global Standards For Governance And Oversight Of Human Genome Editing
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Author : World Health Organization
language : en
Publisher: World Health Organization
Release Date : 2021-09-21
Who Expert Advisory Committee On Developing Global Standards For Governance And Oversight Of Human Genome Editing written by World Health Organization and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-09-21 with Medical categories.
Who Expert Committee On Biological Standardization
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Author : WHO Expert Committee on Biological Standardization. Meeting
language : en
Publisher: World Health Organization
Release Date : 2013
Who Expert Committee On Biological Standardization written by WHO Expert Committee on Biological Standardization. Meeting and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013 with Medical categories.
This report presents the recommendations of a WHO Expert Committee commissioned to coordinate activities leading to the adoption of international recommendations for the production and control of vaccines and other biologicals and the establishment of international biological reference materials. The report starts with a discussion of general issues brought to the attention of the Committee and provides information on the status and development of reference materials for various antibodies, antigens, blood products and related substances, cytokines, growth factors, endocrinological substances and in vitro diagnostic devices. The second part of the report, of particular relevance to manufacturers and national regulatory authorities, contains revised WHO recommendations for production and control of live attenuated influenza vaccines and for production and control of pneumococcal conjugate vaccines. New WHO guidelines on the regulatory evaluation of similar biotherapeutic medicines are also provided. Also included are a list of recommendations, guidelines and other documents for biological substances used in medicine, and of international standards and reference reagent for biological substances.
Who Expert Committee On Specifications For Pharmaceutical Preparations
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Author : WHO Expert Committee on Specifications for Pharmaceutical Preparations. Meeting
language : en
Publisher: World Health Organization
Release Date : 2015-05-11
Who Expert Committee On Specifications For Pharmaceutical Preparations written by WHO Expert Committee on Specifications for Pharmaceutical Preparations. Meeting and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-05-11 with Business & Economics categories.
The World Health Organization (WHO) Expert Committee on Specifications for Pharmaceutical Preparations advises the Director-General of WHO in the area of medicines quality assurance. It provides independent expert recommendations and guidance to ensure that medicines meet standards of quality safety and efficacy in all WHO Member States. Its advice is developed through a broad consensus-building process and covers all areas of quality assurance of medicines from their development to their distribution to patients. In the area of quality control the Expert Committee reviewed new and revised specifications and general texts for inclusion in The International Pharmacopoeia and received the annual report of the European Directorate for the Quality of Medicines & HealthCare (EDQM) the custodian centre for International Chemical Reference Substances (ICRS). The Committee adopted a number of monographs general texts and ICRS. It noted the report on Phase 5 of the External Quality Assurance Assessment Scheme (EQAAS) and on new approaches to ensure sustainability of this scheme through user fees. The Committee further received a concept paper on the benefits of good pharmacopoeial practices (GPhP) and was informed of progress achieved with developing a comprehensive document on GPhP through discussions at consecutive international meetings of world pharmacopoeias. In the various quality assurance-related areas the Expert Committee was presented with a number of new and revised guidelines related to good manufacturing practices (GMP) distribution and trade of pharmaceuticals and regulatory practice. It adopted eight guidelines and 16 technical supplements as listed below including a new guidance text on good review practice prepared under the leadership of the Asian-Pacific Economic Cooperation Regulatory Harmonization Steering Committee. The Committee took note of ongoing work to promote collaboration and information exchange through the good regulatory practice project and welcomed the development of a comprehensive set of guidelines for all national regulatory authorities through this project. The report includes the following annexes which are recommended as new WHO guidelines: . Annex 1. Procedure of the development of monographs for inclusion in The International Pharmacopoeia (revision); . Annex 2. Updating mechanism for the section on radiopharmaceuticals in The International Pharmacopoeia (revision); . Annex 3. Supplementary guidelines on good manufacturing practices: validation; Appendix 7: non-sterile process validation (revision); . Annex 4. General guidance for inspectors on hold-time studies (new); . Annex 6. Recommendations for quality requirements when plant-derived artemisinin is used as a starting material in the production of antimalarial active pharmaceutical ingredients (revision); . Annex 7. Guidelines on registration requirements to establish interchangeability (revision); . Annex 8. Guidance on the selection of comparator pharmaceutical products for equivalence assessment of interchangeable multisource (generic) products (revision); . Annex 9: Good review practices guidelines for regulatory authorities (new). In addition 16 technical supplements to the WHO model guidance for the storage and transport of time- and temperature-sensitive pharmaceutical products were adopted for publication in a format which is appropriate to the large volume of this guidance (Annex 5). The newly adopted monographs were adopted for inclusion in The International Pharmacopoeia. Following the implementation of the revised general monograph on parenteral preparations the Committee adopted the proposed endotoxin limits for 11 parenteral dosage form monographs lacking such specification together with related updates to relevant monographs. The Committee adopted 12 ICRS newly characterized by the custodian centre EDQM. The Committee further adopted the workplan for new monographs to be included in The International Pharmacopoeia.
Who Expert Committee On Biological Standardization
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Author : World Health Organization. Expert Committee on Biological Standardization
language : en
Publisher: World Health Organization
Release Date : 2015-06-30
Who Expert Committee On Biological Standardization written by World Health Organization. Expert Committee on Biological Standardization and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-06-30 with Business & Economics categories.
This report presents the recommendations of a WHO Expert Committee commissioned to coordinate activities leading to the adoption of international recommendations for the production and control of vaccines and other biological substances and the establishment of international biological reference materials. Following a brief introduction the report summarizes a number of general issues brought to the attention of the Committee. The next part of the report of particular relevance to manufacturers and national regulatory authorities outlines the discussions held on the development and adoption of new and revised WHO Recommendations Guidelines and guidance documents. Following these discussions a WHO guidance document on the Scientific principles for regulatory risk evaluation on finding an adventitious agent in a marketed vaccine was adopted along with WHO Guidelines on procedures and data requirements for changes to approved vaccines and revised WHO Recommendations to assure the quality safety and efficacy of poliomyelitis vaccines (inactivated). Subsequent sections of the report provide information on the current status and proposed development of international reference materials in the areas of antibiotics; biotherapeutics other than blood products; blood products and related substances; in vitro diagnostic device reagents; and vaccines and related substances. A series of annexes are then presented which include an updated list of all WHO Recommendations Guidelines and other documents on biological substances used in medicine (Annex 1). The above three WHO documents adopted on the advice of the Committee are then published as part of this report (Annexes 2–4). Finally all additions and discontinuations made during the 2014 meeting to the list of International Standards Reference Reagents and Reference Panels for biological substances maintained by WHO are summarized in Annex 5. The updated full catalogue of WHO International Reference Preparations is available at: http://www.who.int/bloodproducts/catalogue/en/.
Who Expert Committee On Biological Standardization
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Author : WHO Expert Committee on Biological Standardization. Meeting
language : en
Publisher: World Health Organization
Release Date : 2013
Who Expert Committee On Biological Standardization written by WHO Expert Committee on Biological Standardization. Meeting and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013 with Medical categories.
"The WHO Expert Committee on Biological Standardization (ECBS) met in Geneva from 18 to 22 October 2010"--Introduction.
Who Expert Committee On Biological Standardization
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Author : World Health Organization
language : en
Publisher: WHO Technical Report
Release Date : 2014
Who Expert Committee On Biological Standardization written by World Health Organization and has been published by WHO Technical Report this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014 with Medical categories.
This report presents the recommendations of a WHO Expert Committee commissioned to coordinate activities leading to the adoption of international recommendations for the production and control of vaccines and other biological substances, and the establishment of international biological reference materials. Following a brief introduction, the report summarizes a number of general issues brought to the attention of the Committee. The next part of the report, of particular relevance to manufacturers and national regulatory authorities, outlines the discussions held on the development of revised WHO Guidelines. Specific discussions took place on the development of WHO guidance on the nonclinical evaluation of vaccine adjuvants and adjuvanted vaccines; the quality, safety and efficacy of typhoid conjugate vaccines; and the quality, safety and efficacy of biotherapeutic protein products prepared by recombinant DNA technology. Subsequent sections of the report provide information on the current status and proposed development of international reference materials in the areas of vaccines and related substances; blood products and related substances; in vitro diagnostic device reagents; and biotherapeutics other than blood products. A series of annexes are then presented which include an updated list of WHO Recommendations, Guidelines and other documents on biological substances used in medicine (Annex 1), followed by a series of WHO Guidelines adopted on the advice of the Committee (Annexes 2-4). All additions and discontinuations made during the 2013 meeting to the list of International Standards and Reference Panels for biological substances maintained by WHO are summarized in Annex 5.