World of DTC Marketing

APRIL 7, 2021

I have to laugh when I hear that a pharma company is patient-centric because that’s become a slogan to make employees feel good about themselves while the costs of prescription drugs increase every year. drug spending by 9 percent” What about taxpayers? Highest-paid CEOs in 2019: Who made the list from healthcare.

Healthcare 162

Healthcare Healthcare Food and Drug Administration Pharma 162

Legacy MEDSearch

JUNE 19, 2023

The US Food and Drug Administration has approved the use of iTFlow® in blood flow analysis. was founded by two doctors with a mission to “change cardiology with blood flow analysis.” Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry.

FDA 52

FDA Food and Drug Administration Recruitment Physicians 52

PM360

AUGUST 9, 2022

Doctor Docs: Oncologists React to ASCO Educational Material. Another 17% recommended mandating patient recruitment requirements and 14% would like to see the development of a diverse pool of investigators and staff. EPA Administrator Michael Regan said the agency will take more aggressive action against PFAS. Drug Approvals.

Healthcare 52

Healthcare Healthcare Food and Drug Administration FDA 52

Pharmaceutical Technology

APRIL 13, 2023

DCTs in regenerative trials are restricted due to tighter controls of sample collection and administration of gene or cell therapy at home, such as stem cells, which can require injections into the spinal cord. However, there is still some use of remote patient monitoring technologies.

Food and Drug Administration 52

Food and Drug Administration Electronics Healthcare Healthcare 52

pharmaphorum

SEPTEMBER 28, 2022

In March 2020, when the pandemic hit, we had to pause in-person recruitment. Understanding these differences across diverse populations can help doctors and HCPs determine what medication and dosage best fit a patient. Food and Drug Administration (FDA). But that also provided us with an unexpected finding.”

Medicine 98

Medicine Food and Drug Administration Medical FDA 98

pharmaphorum

JANUARY 25, 2023

Digital therapeutics company Woebot Health has announced enrolment of the first patient in a pivotal clinical trial to evaluate the safety and efficacy of WB001, an investigational therapeutic for postpartum depression (PPD), granted Breakthrough Device designation by the US Food and Drug Administration (FDA) in 2021.

Food and Drug Administration 104

Food and Drug Administration Prescription Media Patients 104

Legacy MEDSearch

JUNE 22, 2023

Food and Drug Administration (FDA) clearance to use the Topcon NW400 retinal camera with its EyeArt AI system to automatically detect diabetic retinopathy (DR), adding to the already-cleared usage with Canon CR-2 AF and Canon CR-2 Plus AF cameras. . ” This latest FDA clearance for the EyeArt v2.2.0 sensitivity and 91.1%

FDA 52

FDA Food and Drug Administration Recruitment Marketing 52