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Human neuronal cells: possibilities in drug safety testing

Drug Target Review

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. Ther Innov Regul Sci. Regul Toxicol Pharmacol RTP.

Drugs 111
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The Evolution of Digital Patient Portals: Enhancing Healthcare Access and Engagement

Vial

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.

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BioSpace Movers & Shakers, Dec. 18

The Pharma Data

Martin Carter Professor in Clinical Investigation and Head of the Laboratory of Investigative Dermatology at The Rockefeller University and Weinblatt is the co-director of Clinical Rheumatology at the Brigham and Women’s Hospital. She joined VMS BioMarketing in 2008 and has served as its president and CEO since 2011.

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Article FDA Thank You FDA updates set the stage for broader use of harmonized standards for safety reporting

Agency IQ

FDA updates set the stage for broader use of harmonized standards for safety reporting Though long considered a top priority by regulators, the process to standardize and harmonize the submission of individual case safety reports (ICSRs) has been slow. Periodic Benefit-Risk Evaluation Reports ).

FDA 40
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Let's Quit Sugar With Audiobook – Let's Quit Sugar

The Pharma Data

The trans-fat ban–food regulation and long-term health. Regulation of glucose metabolism from a liver-centric perspective. Clinical Research Strategies for Fructose Metabolism. Measuring visceral and hepatic fat in clinical practice and clinical research. 2008 Nov 4;105(44):17145-50.

Disease 52
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How the Fifty States View Electronic Data as a “Product”

Drug & Device Law

2003), an Internal Revenue Service regulation, excluded liability for “product” refund, repair or replacement. 2008 WL 11344752, at *2 (D. April 22, 2008); Isham v. 2008 WL 2622791, at *4 (N.D. 2008) (all quoting and following Pierson definition of product). at 77 (citation omitted). In United States v.

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Federal Preemption of State Attempts To Ban FDA-Approved Abortion Drugs After Dobbs

Drug & Device Law

In enacting the FDCA, Congress created the FDA and charged it with “promot[ing] the public health by promptly and efficiently reviewing clinical research and taking appropriate action on the marketing of regulated products in a timely manner.” 363, 373 (2000)). Zogenix II , 2014 WL 4273251, at *2 (quoting Savage v.