PSA is a validated FDA-recognized clinical endpoint in assessing prostate cancer treatment response; Telomir-1 lowered PSA levels in a dose-related manner. MIAMI, FLORIDA / ACCESS Newswire / November ...
A senior Food and Drug Administration official on Friday said the agency will change its vaccine approval process.
Parkinson’s Disease (PD) remains the second most prevalent neurodegenerative disorder worldwide, yet it continues to evade a definitive disease-modifying ...
BackgroundOlder adults experience a high burden of acute and chronic pain, often in the context of multimorbidity, frailty, ...
PHILADELPHIA, PENNSYLVANIA / ACCESS Newswire / / Medicus Pharma Ltd. (NASDAQ:MDCX) ("Medicus" or the "Company"), a precision guided biotech/life sciences company focused on advancing the clinical ...
All dollar amounts are in Canadian dollars (“$”) unless otherwise indicated. VANCOUVER, BC, Dec. 1, 2025 /CNW/ – Thesis Gold ...
Opinion
Medical Device Network on MSNOpinion
UK reforms highlight the case for digital submissions in medical device regulation
Diogo Geraldes, director of regulatory strategy, Europe at Veeva MedTech, discusses the potential of digital submissions to benefit manufacturers, regulators, and patients.
The forms, part of the agency’s upgraded CTP Portal Next Generation, let applicants create, validate and submit premarket ...
Robert Maxwell founded a scientific publishing empire after World War II that turned research papers into a profitable business.
A new AI tool, called Festival Fixr, has launched to help independent filmmakers navigate the complex film festival ...
Broadly speaking, international research collaborations continue to rise globally, and Adams says that’s a good thing: the ...
Artificial intelligence tools are boosting researchers’ productivity, but some worry about the effect of a growing reliance ...
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