Remove FDA Remove Medical Records Remove Patient Care
article thumbnail

Philips makes another digital buy, as Thermo adds COVID-19 test maker

pharmaphorum

Between them, Royal Philips and Thermo Fisher have been driving a mini M&A spree in the medical technology sector, snapping up three companies in the last few weeks. Mesa has emergency use authorisation from the FDA for the COVID-19 application and full approvals for the other diseases.

article thumbnail

What is RWE in Pharma?

Viseven

Food and Drug Administration ( FDA ) characterizes RWE as “the clinical evidence regarding the usage and potential benefits or risks of a medical product derived from real-world data analysis.” Viseven helps organizations gain real insight into the world from the point of care throughout the patient journey.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

Real-World Data on Expanding Step-Up Dosing Administration of Bispecific T-Cell Engagers in the Outpatient Setting

Pharmacy Times

The authors examined the safety, feasibility, and toxicity management of delivering both SUD and target doses in outpatient settings, offering institutional guidance for optimizing patient care and reducing hospitalization burden.

article thumbnail

Barriers to Bridging Clinical Trial Data to Routine Pharmacy Practice

Pharmacy Times

A panelist discusses how implementing new clinical trial findings into practice involves multiple challenges including operationalizing treatment regimens in electronic medical records (EMR), procuring medications, obtaining formal approval through institutional committees, and, most significantly, securing insurance approval since insurers often update (..)