Remove 2017 Remove Compliance Remove Informed Consent Remove Public Health
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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

To add to these documents, a template for “Substantial modification of performance study under Regulation (EU) 2017/746” is also provided. A concerted and collaborative effort is essential to address this threat to global health, economies, and security effectively. Tackling AMR is one of ICMRA’s strategic priorities.

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Intersectionality, Indigeneity, and Disability Climate Justice in Nepal

Bill of Health

Located in the Himalayas, Nepal is experiencing increasing temperatures, changing rainfall patterns, glacial retreat, and increasingly frequent and intense climate emergencies; it ranked fourth in the 2017 Global Climate Risk Index of most impacted countries.

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The BFDs – The Ten Best Prescription Drug/Medical Device Decisions of 2023

Drug & Device Law

Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Negligence requires an evaluation of a defendant’s reasonableness, and all relevant NC authority includes relevant regulatory compliance in that mix. Plaintiffs’ own litigation strategy thus opened the door to compliance evidence.

FDA 105