Clarify Health

NOVEMBER 21, 2022

End users of Clarify Trials are typically study team members involved in the design of studies and strategies for recruiting participants, says Drouin. That said, you can identify the places [facilities or the clinicians] where those kinds of individuals were seen” that can then be approached to help recruit them.

Food and Drug Administration 52

Food and Drug Administration Transportation Food Recruitment 52

Legacy MEDSearch

APRIL 25, 2023

Food and Drug Administration (FDA). Proprio’s goal is to dramatically improve clinical and economic outcomes by unlocking both the ability to capture advanced data and the potential of that data to inform more predictive and prescriptive intelligence in surgery.

FDA 52

FDA Food and Drug Administration Recruitment Medical 52

Legacy MEDSearch

JULY 6, 2023

Food and Drug Administration (FDA). This important milestone enables the world’s first prescription music platform, and is a remarkable day for our company, for music, for healthcare, and most importantly for stroke survivors.”

FDA 52

FDA Food and Drug Administration Recruitment Medical 52

Clarify Health

OCTOBER 26, 2021

Food and Drug Administration (FDA) released guidance entitled, Enhancing the Diversity of Clinical Trial Populations — Eligibility Criteria, Enrollment Practices, and Trial Designs Guidance for Industry. To advance equity in clinical research, the U.S. Clarify launched its real-world evidence on health disparities in 2021.

Food and Drug Administration 52

Food and Drug Administration Recruitment Pharmaceutical manufacturing Medical 52

Clarify Health

NOVEMBER 21, 2022

End users of Clarify Trials are typically study team members involved in the design of studies and strategies for recruiting participants, says Drouin. That said, you can identify the places [facilities or the clinicians] where those kinds of individuals were seen” that can then be approached to help recruit them.

Food and Drug Administration 40

Food and Drug Administration Transportation Food Recruitment 40

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 88

Food and Drug Administration Prescription Media FDA 88

MedCity News

JUNE 12, 2023

Combined, DTx and DCTs improve patient recruitment, retention, and access, allowing researchers to pull from underserved communities, including rural populations. If you can get treatment without a prescription, the product price plummets so the seller must make up for that hole with significantly greater sales volume.

Food and Drug Administration 103

Food and Drug Administration Prescription Government FDA 103

Cadensee

JULY 20, 2021

It might be silly question but bringing a drug to market takes many, many years. So, do you listen to them at the point when a pharma company decides what drug it needs to make? Do you listen to them to improve your marketing and the way they should take the drug or the drug should be administered and so on so forth?

Food and Drug Administration 52

Food and Drug Administration Doctors Healthcare Healthcare 52