Drug Administration Software Available In Canada
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based in USA
The medical device reporting (MDR) requirements of 21 CFR 803 apply to manufacturers, importers, distributers, and device user facilities in the United States. Such facilities are required to report adverse device-related events to the Food and Drug Administration (FDA) or the device manufacturer, and occasionally to both. These ...
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based in USA
the Food and Drug Administration's (FDA) design control guidelines. MasterControl offers design control software systems for the design history files (DHF) which are established for each device to house this documentation for the ...
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based in USA
as required by the United States Food and Drug Administration (US FDA) and Health Canada. The US FDA has mandated SPL requirements for over 50 types of documents, and HC has mandated SPM requirements for over 6 types of ...
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by Certarabased in USA
(PMDA), China Food and Drug Administration (CFDA), and the UK Medicines and Healthcare Products Regulatory Agency (MHRA), all use Phoenix WinNonlin to evaluate drug ...
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Manufactured by Stilla Technologiesbased in FRANCE
An increasing number of laboratories are using electronic records and electronic signatures for exchanging and storing data. Electronic documentation offers many benefits, including increased efficiency and productivity when storing data and easier information sharing and data mining. The Food and Drug Administration (FDA) of the United ...
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Manufactured by Finapres Medical Systemsbased in NETHERLANDS
New GAT application enables standardization and quantification! In autonomic testing, standardized procedures are essential for reliable test results. Finapres Medical Systems developed a Guided Autonomic Testing (GAT) application as part of the Finapres® NOVA, which guides the operator and the patient through a series of autonomic test maneuvers. The GAT application consists of a graphical ...
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Manufactured by Finapres Medical Systemsbased in NETHERLANDS
New GAT application enables standardization and quantification! In autonomic testing, standardized procedures are essential for reliable test results. Finapres Medical Systems developed a Guided Autonomic Testing (GAT) application as part of the Finapres® NOVA, which guides the operator and the patient through a series of autonomic test ...
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by Certarabased in USA
The one software ecosystem to streamline your PK/PD data management and analysis; With all the tools you need in a single, interoperable platform, effortlessly share pre-clinical and clinical knowledge across your organization through secure and consistent workflows using Phoenix-based tools and 3rd-party applications. Phoenix WinNonlin is the first choice for non-compartmental analysis (NCA), ...
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Manufactured by 3DHISTECH Ltd.based in HUNGARY
The CaseManager pathology management system gives the pathologist full control of the clinical workflow. CaseManager offers a comprehensive system from digitization through pathologist assignment, primary inspection, additional orders, and consultation to image analysis. CaseManager is the ultimate tool to access and handle all necessary information of the medical cases / that the medical ...
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based in
The multidisciplinary solution for your hospital information ...
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based in USA
Payers, seeking a clearer view into treatment validity, turn to Eviti Connect. Focused on high-quality, high-value care, the platform offers insight payers need to make reimbursement decisions. For payers, Eviti Connect streamlines the authorization of cancer treatment, ensuring prescription of high-quality, high-value care and setting patients on the path to appropriate treatment sooner. ...
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