Results 41 to 50 of about 1,644,868 (275)
A STRATEGIC FRAMEWORK FOR START-UP MEDICAL DEVICE MANUFACTURERS IN SOUTH AFRICA
South African Journal of Industrial Engineering, 2019 An exploratory, qualitative study was conducted to establish why local medical device manufacturing firms are not starting up in South Africa. Semi-structured interviews were conducted with local medical device manufacturers to understand the market and ...
Maharaj, Ishan +1 more
doaj +1 more source
Pharmacovigilance as an imperative of modern medicine - experience from Montenegro [PDF]
Vojnosanitetski Pregled, 2017 nema
Mugoša Snežana +5 more
doaj +1 more source
Medical Benefits from Space Research [PDF]
, 1967 Medical benefits resulting from utilization of devices and techniques of space research within NASA ...
core +1 more source
Therapeutic Apheresis and Dialysis, EarlyView.ABSTRACT Introduction Patients with ovarian cancer often present with massive ascites, leading to significant protein loss during surgical procedures. Although cell‐free concentrated ascites reinfusion therapy (CART) is used in palliative settings to mitigate protein loss, its application in intraoperative settings remains unexplored.
Yutaka Yoneoka +7 more
wiley +1 more source
Registration of medical devices
Perspectives in Clinical Research, 2010 Globally the medical device (MD) market has been growing quite rapidly over the past decade. The regulatory framework for pharmaceuticals and devices differ substantially.
Bobby George
doaj
Materiovigilance Programme of India: A scheme to assure cardiovascular devices safety surveillance
Indian Heart Journal, 2020 The Materiovigilance Programme of India (MvPI) has been implemented to ensure the safety of medical devices including cardiovascular devices (MD-CVD). This article describes the role of MvPI surveillance system that comprehensively collects, collates and
V. Kalaiselvan +2 more
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Pharmacovigilance: Empowering healthcare professionals [PDF]
Hospital Pharmacology, 2015 Introduction: Spontaneous reporting of adverse reactions is of greatest importance for obtaining information about adverse drug reactions (ADRs) after granting the marketing authorization.
Mugoša Snežana S. +5 more
doaj +1 more source
"Regulating Healthcare Technologies and Medical Supplies: A Comparative Overview" [PDF]
, 1995 A complex relationship exists among EU regulations, current national practices and rules, institutional capacities to implement regulatory adjustments and the legacy of past health and regulatory policy and traditions.
Altenstetter, Christa.
core
FEBS Letters, EarlyView.Cryptochrome and PAS/LOV proteins play intricate roles in circadian clocks where they act as both sensors and mediators of protein–protein interactions. Their ubiquitous presence in signaling networks has positioned them as targets for small‐molecule therapeutics. This review provides a structural introduction to these protein families.
Eric D. Brinckman +2 more
wiley +1 more source
On the review of electronic technologies applied to implantable medical devices
Tecnología en Marcha, 2021 The development of electronic implantable medical devices (IMD) has been increasing over the years, targeting very diverse applications and implementing different technologies.
Ronny García-Ramírez +6 more
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