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A Site Management Organization (SMO) is an organization that provides clinical trial-related services to a contract research organization (CRO), a pharmaceutical company, a biotechnology company, a medical device company, or a clinical site.
Contract clinical research for pharmaceutical, biotechnology, medical device, academic and government organizations; services include drug development, laboratory and lifecycle management. Revenue $4.7 Billion (2020) [ 2 ]
2015: ICON acquired MediMedia Pharma Solutions to enhance market access and scientific communications capabilities, and PMG Research Inc., an integrated network of clinical research sites in the US [37] [38] 2016: ICON acquired Clinical Research Management Inc., to extend its presence in the government-sponsored research market [39]
The International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, a 2015 Swiss NGO of pharmaceutical companies and others, defined a contract research organization (CRO), specifically pertaining to clinical trials services as: [8]: 10 "A person or an organization (commercial, academic, or other) contracted by the sponsor to perform one or ...
KCR is a clinical development provider for the biotechnology and pharmaceutical industries. It has three main service areas: Trial Execution, Consulting and Placement. KCR operates across four main regions: North America, Western Europe, Central Europe, and Eastern Europe, with a main operational hub located in Boston, MA, and other hubs in Berlin, Germany, Warsaw, Poland, Kyiv, Ukraine and ...
Characteristics of good clinical research sites include setting good timelines, early participant recruitment, and having a management plan for efficiency. [2] Researchers in nursing have reported challenges accessing the facilities designated for conventional medical research. [3] The design of a research site should have a means of detecting ...
Clinical trial registries are also set up and managed by governmental organizations, non-governmental organizations, universities, as well as commercial and nonprofit entities. This includes pharmaceutical companies, international organizations, and health organizations.
The Clinical Data Interchange Standards Consortium (CDISC) is a standards developing organization (SDO) dealing with medical research data linked with healthcare,made to enable information system interoperability and to improve medical research and related areas of healthcare.