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Expert panel support for orphan medical devices
Expert panel support for orphan medical devices
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Human medicines European public assessment report (EPAR): Amvuttra, vutrisiran, Date of authorisation: 15/09/2022, Revision: 6, Status: Authorised
Human medicines European public assessment report (EPAR): Amvuttra, vutrisiran, Date of authorisation: 15/09/2022, Revision: 6, Status: Authorised
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A Growing Global Push for Free Education for Every Child
Click to expand Image Students in a pre-primary school classroom in Tashkent, Uzbekistan, 2021. © 2021 Bede Sheppard / Human Rights Watch The global push to make free education accessible for every child gained momentum, as 81 states…
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China Wants Citizens to Report ‘Illegal’ Religious Practice
Click to expand Image The eight members of Zion Church who remain detained. Top from left to right: Gao Yingjia, Wang Cong, Wang Lin, Lin ShuchengBottom from left to right: Wu Qiuyu, Liu Zhenbin, Yin Huibin, Wang Zhong…
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Indonesian Military Court Reduces Acid Attack Sentences
Click to expand Image Andrie Yunus, deputy coordinator at KontraS, attending a protest in Bandar Lampung, Sumatra on February 5, 2026. © 2026 Project Multatuli/Adrian Mulya A military court in Jakarta reduced the prison sentences and overturned the…
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Turkey Detains 24 in Belgium-Linked Drug Trafficking Probe
Turkish authorities have detained 24 people and seized assets worth approximately $20.6 million in an operation targeting an international drug trafficking network allegedly directed from Belgium, the Justice Ministry said.The Izmir Chief Public Prosecutor’s Office issued detention warrants…
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Human medicines European public assessment report (EPAR): Qezzaqar, catequentinib, Status: Opinion
Human medicines European public assessment report (EPAR): Qezzaqar, catequentinib, Status: Opinion
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Chapter 3.II: XEVPRM detailed user guidance on the electronic submission of information on medicinal products for human use by marketing authorisation holders to the EMA
Chapter 3.II: XEVPRM detailed user guidance on the electronic submission of information on medicinal products for human use by marketing authorisation holders to the EMA
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