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Medical Software In Singapore
40 software items found
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Manufactured by:Bertin Technologies based inMontigny-le-Bretonneux, FRANCE
The DataEXPERT 10 is a web-based data management software collecting, managing, charting and evaluating data measured by extensive radiological monitoring networks. The powerful and user-friendly web-based interface is available on laptops, computers, but also on smartphones and tablets for mobile use. The data are displayed in charts or tables, with static or dynamic GIS map ...
Manufactured by:Cisa Group S.R.L. based inLucca, ITALY
TraceCare® Cisa Group’s solution for clinical risk reduction. The medical devides traceability and management of processes within the hospital sterilization center (CSSD) is essential. Within the CSSD (Central Sterile Services Department) medical devices and surgical instruments supplies and equipment used for patient care are treated. TraceCare® is the traceability system ...
Manufactured by:Applied Satellite Technology Asia Pte Ltd (AST) based in, SINGAPORE
IRIS is an award-winning, cost-efficient satellite communications remote asset tracking system for control and monitoring IoT over satellite, enabling users to unlock the true potential of IoT and M2M. The application is versatile and customisable and is suitable for a wide range of uses from, remote pressure and sensor monitoring to animal and personnel ...
by:Novatek International based inMontreal, QUEBEC (CANADA)
In clinical studies, assessing and managing risks, as well as establishing areas of uncertainty that contribute to risk, are critical to a company’s decision making processes. Many business units within pharmaceutical, biotechnology and clinical research organizations must comply with federal regulations concerning their processes and computerized systems. One of the most challenging ...
by:Novatek International based inMontreal, QUEBEC (CANADA)
All healthcare and life science organizations that develop and manufacture products rely greatly on accurate informative text and printed labels to communicate to their end user and build their product brands successfully. Novatek’s software provides effective proof reading results to support the industry’s highest standards; eliminating printing errors in all product information ...
Manufactured by:Ortho Clinical Diagnostics based in, SINGAPORE
Software Designed To Standardize Lab Operations, Simplify Repetitive Tasks And Deliver Improved Productivity So You Can Focus On Providing The Best Patient Care. Because Every Test Is A LifeTM Take Lab Productivity To The Next Level. ORTHO CONNECT® Software enables centralized workflow automation and sample management in blood banks. With it, you can leverage data and metrics to optimize ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
Data sourced from the EHRs of U.S. healthcare organizations forms the foundation of this combined data asset, providing a rich clinical picture of patients from encounters with providers, lab results, procedures, medication orders, and genomics. Medical and pharmacy claims provide insight into a patient’s care before and after these encounters, regardless of provider. Pre-existing ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
The full set of base analytics are enabled on every network, except for anonymous networks such as Linked, where HCO attribution is not shown. With Explore Cohort, review the prevalence of diagnoses, treatments, and procedures among your cohort, retrieve lab value means and standard deviations, and count instances of variants by genome. Use Criteria Analysis to rank order your query ...
Manufactured by:Perspectum based inOxford, UNITED KINGDOM
Hepatica is a clinical and surgical decision support tool based on non-invasive quantitative multiparametric MRI. It enables more informed preoperative decision making and better risk-stratification, therefore improving post-operative outcomes. It does this by providing simultaneous evaluation of liver health (fibroinflammation and fat) and volumetry with AI-driven delineation of the liver and ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
Document change control software is essential for ensuring compliance and managing change in regulated industries such as life sciences and manufacturing. By utilizing this software, companies can effectively address the complexity of change control and streamline their ...
by:Novatek International based inMontreal, QUEBEC (CANADA)
Successful innovation programs more and more key to driving corporate growth and maintaining competitive advantage. Innovation programs must be sustainable and agile to keep pace with today’s rapidly changing environments. Companies struggle with how to establish and sustain the innovation process. Persons within the organization are an excellent resource for new ideas. Organizations ...
Manufactured by:Cisa Group S.R.L. based inLucca, ITALY
TraceCare® system offers a number of packages depending on the customer’s needs. MONITORING: The Monitoring version allows the monitoring and saving of the cycles of the machines present within the CSSD. Data concerning the main cycle parameters are saved in the DataBase and can be displayed as graphs or shown in summary reports. The communication between TraceCare® and the PLC ...
by:Lisam Systems based inEcaussinnes, BELGIUM
Create and maintain the Cosmetic PIFs for your products. Our regulatory software enables you to create and maintain the necessary Product Information Files (PIF) for all your cosmetic products. Our application supports to manage the PIF's completely by yourself. When required, we can also create and sign the PIF for ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
TriNetX Open Claims data sets are built to close data gaps and provide insights throughout the product lifecycle, including market analysis and forecasting. Claims are sourced from clearinghouses that have processed more than 4 billion medical and pharmacy claims for over 300M patients since 2014; data is refreshed daily to enable an up-to-date understanding of market access and treatment ...
Manufactured by:Perspectum based inOxford, UNITED KINGDOM
The Perspectum Portal is the interface through which our quantitative analysis service is delivered to customers. Clinicians and radiologists can upload patient MRI scans to this secure, user-friendly platform and easily monitor analytical progress, before receiving a downloadable digital ...
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 ...
Manufactured by:Industrial Minerva Sdn Bhd based inKembangan, MALAYSIA
Harness the best in Telemetry, M2M and Internet of Things solutions to optimize your operations, increase safety and reduce carbon ...
by:Partek Incorporated based inChesterfield, MISSOURI (USA)
Partek® Pathway™ allows you to explore complex biological relationships and pathways between genes to discover meaningful biological insights. You can calculate pathway enrichment, detect disrupted or influential pathways, search for specific pathways and genes, and color code genes based on their p-values and fold changes. Partek Pathway integrates inside Partek Flow or Partek Genomics ...
by:MasterControl, Inc based inSalt Lake City, UTAH (USA)
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict conformance to approved specifications which can be acheived easily ...
by:TriNetX, LLC based inCambridge, MASSACHUSETTS (USA)
Trials that include patients in Japan have an advantage when it comes to regulatory approval in that country, where pharmaceutical sales reached 94B USD in 2020. But approval requires promising results from a well-executed study. Start the process the right way by understanding Japan's patient population, designing a feasible study, and selecting the right trial sites. ...