pharmaphorum3d
When measuring European regulatory approval, the timestamp matters
specifically in comparing approval regulatory cycles for the Food and Drug Administration (FDA) and the European Medicines Agency (EMA). Last year we wrote a three-part series, "Life in the Fast ...
Hosted on MSN2d
Neurizon's fast-track application for flagship drug in Europe received 'positively'
While the final decision is set for next month, biotech player Neurizon’s (ASX:NUZ) hopes have been lifted with a view ...
Yahoo Finance6d
Uptime Launches Enhanced M&O Stamp of Approval to Accelerate Improvements in Data Center Operational Resiliency
Seven New Scope Areas and Proprietary Staff Assessment Tool Help Clients Strengthen Operational Excellence, Minimize Human Error, and Improve Workforce Skills NEW YORK, November 07, 2024 ...
It News Online6d
Uptime Launches Enhanced M&O Stamp of Approval to Accelerate Improvements in Data Center Operational Resiliency
Uptime Institute today announced its newly enhanced, market-leading, and globally adopted Management & Operations (M&O) Stamp of Approval. The extensive enhancements will improve clients’ ability to ...
Business Wire5d
Uptime Launches Enhanced M&O Stamp of Approval to Accelerate Improvements in Data Center Operational Resiliency
Uptime Institute today announced its newly enhanced, market-leading, and globally adopted Management & Operations (M&O) Stamp of Approval. The extensive enhancements will improve clients ...
WBEZ5d
Illinois voters give stamp of approval on three nonbinding referendums
Voters backed enhanced election security, healthcare coverage for IVF and a so-called millionaire’s tax to fund property tax relief. Illinois voters got to weigh in on three nonbinding ...
CBS News6d
European agency says 2024 is "virtually certain" to be warmest year on record
Climate scientists working at the European Union's Copernicus Climate ... According to its ERA5 dataset, the agency said it was "virtually certain" that the annual temperature for 2024 will ...
CBS News5d
FDA to pull common but ineffective cold medicine from market
The Food and Drug Administration announced Wednesday that it would seek to pull a widely used ingredient in cough and cold medicines from the market, after the ... support its approval and new ...
New York Daily News5d
50 European leaders assess how Trump will affect their fortunes and seek a common stance on Russia
BUDAPEST, Hungary (AP) — Around 50 European leaders on Thursday called for a stronger defense posture across the continent that no longer necessitates a fundamental dependence on Washington as ...
devdiscourse1d
Aurobindo Pharma's Triumph: EU GMP Certification for Biosimilars
Aurobindo Pharma's subsidiary, CuraTeQ Biologics, has received a GMP certificate from the European Medicines Agency for its ...
manilatimes6d
SYNDEO Medical Announces European MDR Approval for Two Product Brands
SYNDEOPack Interventional Procedure Packs™ and Xssential Rapid Delivery Procedure Packs™, have received European Medical Device Regulation (MDR) approval. "We have observed over the years that the ...
Politico Europe6d
Belgium’s Lahbib approved by Parliament as new EU crisis management boss
Commissioner-designate for Preparedness, Crisis Management, and Equality, Hadja Lahbib, got the green light by Members of European Parliament on Wednesday afternoon, she announced on her X account.