The Pharma Data

MAY 2, 2023

Bonello has more than 30 years of financial leadership experience, including 15 years in the clinical research industry. a clinical trial data collection company, since 2021. From 2008 to 2021, Mr. Bonello held roles of increasing responsibility at Nasdaq-listed PRA Health Sciences, Inc.,

Clinical Trials 40

Clinical Trials Clinical Research Science Clinical Development 40

Vial

FEBRUARY 23, 2024

In 2022, the global market value of patient portals within the clinical research and healthcare industries was estimated to be US $2.9 In 2008, prior to ARRA and the HITECH Act, only 10% of hospitals in the United States had transitioned from paper-based methods into EMRs, primarily due to their exorbitant set-up costs.

Clinical Trials 52

Clinical Trials Clinical Research Trials Hospitals 52

Quanticate

OCTOBER 16, 2020

By the end of 2007, and towards the beginning of 2008, the Clinical Data Interchange Standards Consortium (CDISC) gained ground in its mission to develop a global set of standards. Gathering all the heterogenous data and mapping to the internal standards of the pharma companies proved to be the greatest challenge of the time.

Pharma Companies 52

Pharma Companies FDA International Drugs 52

Drug Target Review

SEPTEMBER 26, 2023

She completed a PhD at Durham University which focused on investigating the mechanisms of cardiotoxicity of cancer therapies using clinically relevant in vitro human models of cardiac physiology paired with novel methodologies to evaluate structural and functional toxicities. 2008 Mar;153 Suppl 2(Suppl 2):S1-209. cited 2023 Jun 15].

Drugs 111

Drugs FDA Disease Animal Testing 111

The Pharma Data

NOVEMBER 5, 2020

Prior to joining Navitor, Hughes served as president and CSO of Zafgen and previously led Zafgen as CEO from 2008 to 2017. State University, will have overall responsibility for the scientific and clinical strategy, including scientific and clinical affairs. Hughes, CEO of Navitor Pharmaceuticals, to the board of directors.

Analytical Chemistry 40

Analytical Chemistry Pharmaceuticals Small Molecule Therapies 40

Agency IQ

APRIL 8, 2024

In 2012, the passage of the FDA Safety and Innovation Act (FDASIA) created a new requirement for sponsors to submit all drug submissions, including clinical trial applications, in an electronic format as specified by FDA guidance. This was an area that FDA investigators recently interviewed by the U.S.

FDA 40

FDA Production Regulations Vaccine 40

The Pharma Data

MAY 13, 2021

based weight loss intervention in adults with obesity: A randomized clinical trial. Clinical Research Strategies for Fructose Metabolism. Reduced Reward-driven Eating Accounts for the Impact of a Mindfulness-Based Diet and Exercise Intervention on Weight Loss: Data from the SHINE Randomized Controlled Trial.

Disease 52

Disease Production Testimonials Science 52