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11 software items found
by:Certara based inPrinceton, NEW JERSEY (USA)
PK/PD and non-compartmental analyses can be time consuming, requiring detailed attention to every step from data preparation to report generation. Phoenix WinNonlin™’s integrated tools for data processing, graphing & charting, report generation, and compliance create an efficient, all-in-one collaboration workbench. Phoenix WinNonlin is used by over 10,000 scientists at more than ...
by:RegScan - by Enhesa based inWilliamsport, PENNSYLVANIA (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 requirements are supplemental to the quality system requirements of ...
Manufactured by:Finapres Medical Systems based inEnschede, 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 ...
Manufactured by:Finapres Medical Systems based inEnschede, 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 ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
Small Medical Device Companies Can Now Manage and Automate their Design Control Process to Ensure Compliance with 21 CFR Part 820 with the Help of MasterControl's Design Control Software Systems at a Low Monthly Cost. Each manufactured medical device must be supported by appropriate documentation which demonstrates that its development followed the Food and Drug Administration's (FDA) design ...
by:Certara based inPrinceton, NEW JERSEY (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), ...
Manufactured by:Stilla Technologies based inVillejuif, 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 States (USA) regulates the food and drug industry of the USA ...
by:Evolucare Technologies Shenzhen Co., Ltd based inFutian District, CHINA
The multidisciplinary solution for your hospital information ...
Manufactured by:3DHISTECH Ltd. based inBudapest, 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 ...
by:AWS Truepower, LLC based inAlbany, NEW YORK (USA)
Discover how our validated, FDA CFR Part 11 compliance training management system helps you comply with evolving FDA Regulations. Keep your workforce up to date. Medical device and pharmaceutical manufacturers trying to keep up with ever-changing regulations have a tough job. Medical technology advances quickly, and with it the need for compliance systems to support patient safety. To help you ...
by:NantHealth, Inc. based inMorrisville, NORTH CAROLINA (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. ...