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Digital Inclusion As Upstream Health Investment

Health Populi

Note the timing of this publication: the authors submitted the manuscript to Nature on 19th March 2020… just eight days after the World Health Organization declared the coronavirus a global pandemic.

COVID-19 154
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Eliminating Trachoma with the Help of GIS Technology

Healthcare IT Today

According to the World Health Organization (WHO), trachoma is “hyperendemic in many of the poorest and most rural areas of Africa, Central and South America, Asia, Australia, and the Middle East”. On September 21 st , 2022 the WHO officially announced that the country had eliminated the disease as a public health problem.

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SQA Regulatory Surveillance Summary | Monthly Update 2022 – September/October

SQA

26 of 2014. It will also facilitate cross-border circulation of these critical health therapies as well as cross-border cooperation between public health authorities. Issuance of a device filing number via a “Notification of Filing Number,” which replaces the current Filing Certificate.

FDA 40
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Report: How Apple Is Advancing Digital Healthcare Transformation

HIT Consultant

. – The report covers Apple’s two-pronged approach to advance health: Apple’s focus on personal health and fitness features on Apple Watch and iPhone, and Apple’s work with the medical community to support research and care. Empowering Users on Their Personal Health Journeys. Keeping Privacy in Mind.

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Dr. Eunice Brookman-Amissah: A Pioneer in Safe Abortion Law Reform

Bill of Health

She then served as Ghana’s Minister of Health from 1996 to 1998 and as Ghana’s Ambassador to the Netherlands from 1998 to 2001. From Minister to Advocate Dr. Brookman-Amissah returned to Ipas in 2001, where she served as Vice President for Africa until 2014.

Doctors 113
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SQA Regulatory Surveillance Summary 3 | Monthly Update 2021

SQA

726/2004, the Commission can grant a duplicate marketing authorization: If there are objective, verifiable reasons relating to public health that show an increased availability of medicinal products to healthcare professionals and/or patients. World Health Organization (WHO). Under Article 82(1) of Regulation (EC) No.

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SQA Regulatory Surveillance Summary for May and June 2024

SQA

NPMA Issues Draft Guidelines for Inspection of Medical Device Clinical Trial Sites, 14 June 2024 China NMPA has released a new guideline that aims to enhance the management of clinical trial institutions for medical devices, ensuring compliance with regulatory standards and safeguarding public health.

FDA 52