GenesisLab360, a laboratory information management system (LIMS), the strongest and more flexible LIMS/LIS Platform that is tailored not only to manage an organization´s laboratory information but to provide an integrated informatics solution and platform that allow for outstanding laboratory capabilities for workflow management, optimizing productivity and operating cost with increasing quality.
Ctrl Vision is a module for monitoring and managing incoming and outgoing production quality levels. Based on ISO2859 and ISO3951 quality standards, Ctrl Vision allows you to confidently accept or reject production batches using proven data driven methods.
An introduction to Life Sciences Computer System Validation, applicable regulation, SDLC phases, software categorisation, risk/ change/ deviation management, validation deliverable, risk based approach, regulatory inspection, audit findings, causes of compliance failure, key concepts in CSV etc.
Process and Regulated Processes Software Validation ElementsArta Doci
Medical device manufacturers operate in a competitive marketplace with increasing end-user demands for features and usability and in a highly regulated environment.
Regulatory bodies look for evidence that medical devices are developed under a structured, quality-oriented development process. By following software validation and verification best practices, one can not only increase the likelihood that they will meet their compliance goals, they can also enhance developer productivity.
Overview on “Computer System Validation” CSVAnil Sharma
HI this is Anil Sharma, Executive Compliance in USV LTD. I want to share my brief knowledge on CSV with you. I hope my presentation will help you to understand basics of CSV.
This Presentation gives an idea about validation and different type of validation and overview of computer system/software validation and basics steps for computer system validations as per the regulatory and user requirement specifications.
Ctrl Vision is a module for monitoring and managing incoming and outgoing production quality levels. Based on ISO2859 and ISO3951 quality standards, Ctrl Vision allows you to confidently accept or reject production batches using proven data driven methods.
An introduction to Life Sciences Computer System Validation, applicable regulation, SDLC phases, software categorisation, risk/ change/ deviation management, validation deliverable, risk based approach, regulatory inspection, audit findings, causes of compliance failure, key concepts in CSV etc.
Process and Regulated Processes Software Validation ElementsArta Doci
Medical device manufacturers operate in a competitive marketplace with increasing end-user demands for features and usability and in a highly regulated environment.
Regulatory bodies look for evidence that medical devices are developed under a structured, quality-oriented development process. By following software validation and verification best practices, one can not only increase the likelihood that they will meet their compliance goals, they can also enhance developer productivity.
Overview on “Computer System Validation” CSVAnil Sharma
HI this is Anil Sharma, Executive Compliance in USV LTD. I want to share my brief knowledge on CSV with you. I hope my presentation will help you to understand basics of CSV.
This Presentation gives an idea about validation and different type of validation and overview of computer system/software validation and basics steps for computer system validations as per the regulatory and user requirement specifications.
Keeping up with the fast-evolving world of trends means that smart work with innovation is required. Having a smart-infrastructure built on informatics solutions can benefit the lab by implementing automation. Laboratory Information Management System (LIMS) is a critical part of the system to be incorporated in all functioning laboratories for better results.
Computerized System Validation Business Intelligence SolutionsDigital-360
Executive Summary
Regulated pharmaceutical, biotech and medical device companies are challenged to develop manufacturing capabilities quickly and cost-effectively while at the same time safeguarding product quality and patient safety.
Validation has been an essential part of regulated industries for over 20 years, yet as the field has evolved, little has changed in the business, or manual, approach to validation.
In this webinar, we will be covering what exactly an SaMDs, or Software as a Medical Device, and go over some examples with Artificial Intelligence. We will also look at Artificial Intelligence and Machine Learning versus the traditional software. Next, we will go into the regulatory framework for these types of software, then explain how EMMA International can help you get your SaMD to market.
Werardt offers various systems like, ERP, Plant Maintenance, Sales & Distribution, etc. to the Industry apart from specialized systems for the past 15 years.
I C M - The Instrument Calibration Management System is a comprehensive, easy-to-use SOFTWARE solution with the ability to maintain long term, organized, and readily accessible calibration records of all types of Instruments.
Many comprehensive reports are generated including Master Calibration Planner.
Please contact Werardt Systemss Pvt Ltd., Pune, India. Phone : 91-20-25285256, 25285257. email: business@werardt.com
Computer System Validation (CSV) is a core requirement for several industries. The aim of Computer System Validation is to ensure, through documentation, that the computer systems function the way they are intended to, consistently, repeatedly and reproducibly, somewhat in the manner expected of scientific experiments. So, the validation, meaning authentication or corroboration, is something that has to be done right from the start, that is, defining the computer system, to their use and going all the way right up to the time the computer system is retired.
CODEX Validation Group is a consulting company with broad experience in the cGMP, compliance, automation, and validation for the Pharmaceutical, Biotechnology and Medical Device industries committed to follow the highest ethical standards as we work with our customers.
Enterprise Asset Management- Mobility Readiness ChecklistUnvired Inc.
We have prepared a comprehensive checklist that helps you with your mobility readiness check for Enterprise Asset Management. Unvired mobility checklist for Enterprise Asset Management is a compilation of experience in implementing Mobile EAM for more than a decade across the globe.
21CFR regulations & its applicability in the industry and FDA perspective on the same and FDA check points on 21CFR regulations during their inspection.
These ready to use LIMS are designed for versatility, security, accessibility ensuring any time connectivity over
a secure web network interface, cross platform and cross database compatibility with customization
possibilities. Well established research organizations and laboratories choose to implement enterprise edition
of LIMS after a lot of deliberation and for a bunch of good reasons
Keeping up with the fast-evolving world of trends means that smart work with innovation is required. Having a smart-infrastructure built on informatics solutions can benefit the lab by implementing automation. Laboratory Information Management System (LIMS) is a critical part of the system to be incorporated in all functioning laboratories for better results.
Computerized System Validation Business Intelligence SolutionsDigital-360
Executive Summary
Regulated pharmaceutical, biotech and medical device companies are challenged to develop manufacturing capabilities quickly and cost-effectively while at the same time safeguarding product quality and patient safety.
Validation has been an essential part of regulated industries for over 20 years, yet as the field has evolved, little has changed in the business, or manual, approach to validation.
In this webinar, we will be covering what exactly an SaMDs, or Software as a Medical Device, and go over some examples with Artificial Intelligence. We will also look at Artificial Intelligence and Machine Learning versus the traditional software. Next, we will go into the regulatory framework for these types of software, then explain how EMMA International can help you get your SaMD to market.
Werardt offers various systems like, ERP, Plant Maintenance, Sales & Distribution, etc. to the Industry apart from specialized systems for the past 15 years.
I C M - The Instrument Calibration Management System is a comprehensive, easy-to-use SOFTWARE solution with the ability to maintain long term, organized, and readily accessible calibration records of all types of Instruments.
Many comprehensive reports are generated including Master Calibration Planner.
Please contact Werardt Systemss Pvt Ltd., Pune, India. Phone : 91-20-25285256, 25285257. email: business@werardt.com
Computer System Validation (CSV) is a core requirement for several industries. The aim of Computer System Validation is to ensure, through documentation, that the computer systems function the way they are intended to, consistently, repeatedly and reproducibly, somewhat in the manner expected of scientific experiments. So, the validation, meaning authentication or corroboration, is something that has to be done right from the start, that is, defining the computer system, to their use and going all the way right up to the time the computer system is retired.
CODEX Validation Group is a consulting company with broad experience in the cGMP, compliance, automation, and validation for the Pharmaceutical, Biotechnology and Medical Device industries committed to follow the highest ethical standards as we work with our customers.
Enterprise Asset Management- Mobility Readiness ChecklistUnvired Inc.
We have prepared a comprehensive checklist that helps you with your mobility readiness check for Enterprise Asset Management. Unvired mobility checklist for Enterprise Asset Management is a compilation of experience in implementing Mobile EAM for more than a decade across the globe.
21CFR regulations & its applicability in the industry and FDA perspective on the same and FDA check points on 21CFR regulations during their inspection.
These ready to use LIMS are designed for versatility, security, accessibility ensuring any time connectivity over
a secure web network interface, cross platform and cross database compatibility with customization
possibilities. Well established research organizations and laboratories choose to implement enterprise edition
of LIMS after a lot of deliberation and for a bunch of good reasons
Automated Test Equipment’s (ATEs) are integrated systems which automate the process of testing modules, systems, devices or products. Test equipment are generally used to monitor and control the operation of a process or device, verify compliance standards, and detect and mitigate risks.
20 Simple Questions from Exactpro for Your Enjoyment This Holiday SeasonIosif Itkin
Warmest wishes for a happy holiday season and a wonderful New Year!
We look forward to our continued collaboration in 2020. Thank you for your support.
Drish Infotech - Lab Information Management System LIMSKaran Checker
Drish Infotech - Lab Information Management System LIMS
A process management IT system for QA labs at pharmaceutical, chemical, food related or other manufacturing facilities.
Includes
- Order Booking
- Sample Receiving and Booking
- Testing and Report generation
- Invoice generation
- Status updation/notification
GLab360 a laboratory information management system and electronic laboratory network document from GTS Systems healthcare and business solution provider
LIMS from WINGLO
Sample Tracking: LIMS allows for the tracking of samples throughout their lifecycle, from collection to analysis and storage. This helps in maintaining the integrity of data associated with each sample.
Data Management: LIMS facilitates the organization and storage of various types of data, including test results, experiment details, and sample information. It often includes tools for data analysis and reporting.
Workflow Automation: LIMS can automate and streamline laboratory workflows, reducing manual errors and improving overall efficiency. This includes automated scheduling, sample processing, and data validation.
Inventory Management: LIMS helps in managing laboratory inventory, including reagents, consumables, and equipment. This ensures that the laboratory has the necessary resources for experiments and tests.
Audit Trail: LIMS typically includes an audit trail feature that tracks changes made to data, ensuring accountability and compliance with regulatory standards.
Integration with Instruments: LIMS can be integrated with various laboratory instruments, allowing for direct data transfer and reducing the risk of transcription errors.
User Access Control: LIMS provides role-based access control, ensuring that only authorized personnel have access to sensitive data and functionalities.
Compliance and Reporting: LIMS helps laboratories adhere to regulatory requirements by providing tools for compliance monitoring and generating reports for regulatory submissions.
Overall, LIMS plays a crucial role in modern laboratories by improving efficiency, data accuracy, and compliance with industry regulations.
Whether you're looking for your first calibration management program or looking to upgrade from a current system, you'll find that Labsols CALIBRATION LIMS has everything you need.
1. Manage Calibration Process and Operation flow
2. Manage Sales Process (Sales Order to Shipment to Billing)
3. Manage Lab Standards/Master Products
4. Manage Lab Staff workload and lab performance
5. Manage Calibration documents and communication
6. Manage Lab Customers and connected to them all time
Completely customized to your current business and lab operations (sales order, batch calibrations, sampling, result entry, multiple-bespoke reports, shipment, billing, document management, KPI, and more)
Comes with Intelligent integration of calibration customer facing portal and mobile apps.
Why should you invest in a Lab Information Management SystemPragadeesh Suresh
A Lab Management Software is simply a tool that can ease the operations involved in modern laboratories by automating most of them. As an all-inclusive software including lab management system, ERP tools, data analytics tool and virtual software, LIMS efficiently works out on the laboratory informatics.
Why should you invest in a Lab Information Management System?MocDoc
A Lab Management Software is simply a tool that can ease the operations involved in modern laboratories by automating most of them. As an all-inclusive software including lab management system, ERP tools, data analytics tool and virtual software, LIMS efficiently works out on the laboratory informatics. While each of the operations involved in LIMS is possible manually, why should one choose the software? Here is why:
https://mocdoc.in/blog/why-should-you-invest-in-a-lab-information-management-system
Cyaniclab : Software Development Agency Portfolio.pdfCyanic lab
CyanicLab, an offshore custom software development company based in Sweden,India, Finland, is your go-to partner for startup development and innovative web design solutions. Our expert team specializes in crafting cutting-edge software tailored to meet the unique needs of startups and established enterprises alike. From conceptualization to execution, we offer comprehensive services including web and mobile app development, UI/UX design, and ongoing software maintenance. Ready to elevate your business? Contact CyanicLab today and let us propel your vision to success with our top-notch IT solutions.
Prosigns: Transforming Business with Tailored Technology SolutionsProsigns
Unlocking Business Potential: Tailored Technology Solutions by Prosigns
Discover how Prosigns, a leading technology solutions provider, partners with businesses to drive innovation and success. Our presentation showcases our comprehensive range of services, including custom software development, web and mobile app development, AI & ML solutions, blockchain integration, DevOps services, and Microsoft Dynamics 365 support.
Custom Software Development: Prosigns specializes in creating bespoke software solutions that cater to your unique business needs. Our team of experts works closely with you to understand your requirements and deliver tailor-made software that enhances efficiency and drives growth.
Web and Mobile App Development: From responsive websites to intuitive mobile applications, Prosigns develops cutting-edge solutions that engage users and deliver seamless experiences across devices.
AI & ML Solutions: Harnessing the power of Artificial Intelligence and Machine Learning, Prosigns provides smart solutions that automate processes, provide valuable insights, and drive informed decision-making.
Blockchain Integration: Prosigns offers comprehensive blockchain solutions, including development, integration, and consulting services, enabling businesses to leverage blockchain technology for enhanced security, transparency, and efficiency.
DevOps Services: Prosigns' DevOps services streamline development and operations processes, ensuring faster and more reliable software delivery through automation and continuous integration.
Microsoft Dynamics 365 Support: Prosigns provides comprehensive support and maintenance services for Microsoft Dynamics 365, ensuring your system is always up-to-date, secure, and running smoothly.
Learn how our collaborative approach and dedication to excellence help businesses achieve their goals and stay ahead in today's digital landscape. From concept to deployment, Prosigns is your trusted partner for transforming ideas into reality and unlocking the full potential of your business.
Join us on a journey of innovation and growth. Let's partner for success with Prosigns.
May Marketo Masterclass, London MUG May 22 2024.pdfAdele Miller
Can't make Adobe Summit in Vegas? No sweat because the EMEA Marketo Engage Champions are coming to London to share their Summit sessions, insights and more!
This is a MUG with a twist you don't want to miss.
Providing Globus Services to Users of JASMIN for Environmental Data AnalysisGlobus
JASMIN is the UK’s high-performance data analysis platform for environmental science, operated by STFC on behalf of the UK Natural Environment Research Council (NERC). In addition to its role in hosting the CEDA Archive (NERC’s long-term repository for climate, atmospheric science & Earth observation data in the UK), JASMIN provides a collaborative platform to a community of around 2,000 scientists in the UK and beyond, providing nearly 400 environmental science projects with working space, compute resources and tools to facilitate their work. High-performance data transfer into and out of JASMIN has always been a key feature, with many scientists bringing model outputs from supercomputers elsewhere in the UK, to analyse against observational or other model data in the CEDA Archive. A growing number of JASMIN users are now realising the benefits of using the Globus service to provide reliable and efficient data movement and other tasks in this and other contexts. Further use cases involve long-distance (intercontinental) transfers to and from JASMIN, and collecting results from a mobile atmospheric radar system, pushing data to JASMIN via a lightweight Globus deployment. We provide details of how Globus fits into our current infrastructure, our experience of the recent migration to GCSv5.4, and of our interest in developing use of the wider ecosystem of Globus services for the benefit of our user community.
How to Position Your Globus Data Portal for Success Ten Good PracticesGlobus
Science gateways allow science and engineering communities to access shared data, software, computing services, and instruments. Science gateways have gained a lot of traction in the last twenty years, as evidenced by projects such as the Science Gateways Community Institute (SGCI) and the Center of Excellence on Science Gateways (SGX3) in the US, The Australian Research Data Commons (ARDC) and its platforms in Australia, and the projects around Virtual Research Environments in Europe. A few mature frameworks have evolved with their different strengths and foci and have been taken up by a larger community such as the Globus Data Portal, Hubzero, Tapis, and Galaxy. However, even when gateways are built on successful frameworks, they continue to face the challenges of ongoing maintenance costs and how to meet the ever-expanding needs of the community they serve with enhanced features. It is not uncommon that gateways with compelling use cases are nonetheless unable to get past the prototype phase and become a full production service, or if they do, they don't survive more than a couple of years. While there is no guaranteed pathway to success, it seems likely that for any gateway there is a need for a strong community and/or solid funding streams to create and sustain its success. With over twenty years of examples to draw from, this presentation goes into detail for ten factors common to successful and enduring gateways that effectively serve as best practices for any new or developing gateway.
Large Language Models and the End of ProgrammingMatt Welsh
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In software engineering, the right architecture is essential for robust, scalable platforms. Wix has undergone a pivotal shift from event sourcing to a CRUD-based model for its microservices. This talk will chart the course of this pivotal journey.
Event sourcing, which records state changes as immutable events, provided robust auditing and "time travel" debugging for Wix Stores' microservices. Despite its benefits, the complexity it introduced in state management slowed development. Wix responded by adopting a simpler, unified CRUD model. This talk will explore the challenges of event sourcing and the advantages of Wix's new "CRUD on steroids" approach, which streamlines API integration and domain event management while preserving data integrity and system resilience.
Participants will gain valuable insights into Wix's strategies for ensuring atomicity in database updates and event production, as well as caching, materialization, and performance optimization techniques within a distributed system.
Join us to discover how Wix has mastered the art of balancing simplicity and extensibility, and learn how the re-adoption of the modest CRUD has turbocharged their development velocity, resilience, and scalability in a high-growth environment.
top nidhi software solution freedownloadvrstrong314
This presentation emphasizes the importance of data security and legal compliance for Nidhi companies in India. It highlights how online Nidhi software solutions, like Vector Nidhi Software, offer advanced features tailored to these needs. Key aspects include encryption, access controls, and audit trails to ensure data security. The software complies with regulatory guidelines from the MCA and RBI and adheres to Nidhi Rules, 2014. With customizable, user-friendly interfaces and real-time features, these Nidhi software solutions enhance efficiency, support growth, and provide exceptional member services. The presentation concludes with contact information for further inquiries.
Enterprise Resource Planning System includes various modules that reduce any business's workload. Additionally, it organizes the workflows, which drives towards enhancing productivity. Here are a detailed explanation of the ERP modules. Going through the points will help you understand how the software is changing the work dynamics.
To know more details here: https://blogs.nyggs.com/nyggs/enterprise-resource-planning-erp-system-modules/
Enhancing Research Orchestration Capabilities at ORNL.pdfGlobus
Cross-facility research orchestration comes with ever-changing constraints regarding the availability and suitability of various compute and data resources. In short, a flexible data and processing fabric is needed to enable the dynamic redirection of data and compute tasks throughout the lifecycle of an experiment. In this talk, we illustrate how we easily leveraged Globus services to instrument the ACE research testbed at the Oak Ridge Leadership Computing Facility with flexible data and task orchestration capabilities.
Navigating the Metaverse: A Journey into Virtual Evolution"Donna Lenk
Join us for an exploration of the Metaverse's evolution, where innovation meets imagination. Discover new dimensions of virtual events, engage with thought-provoking discussions, and witness the transformative power of digital realms."
Globus Compute wth IRI Workflows - GlobusWorld 2024Globus
As part of the DOE Integrated Research Infrastructure (IRI) program, NERSC at Lawrence Berkeley National Lab and ALCF at Argonne National Lab are working closely with General Atomics on accelerating the computing requirements of the DIII-D experiment. As part of the work the team is investigating ways to speedup the time to solution for many different parts of the DIII-D workflow including how they run jobs on HPC systems. One of these routes is looking at Globus Compute as a way to replace the current method for managing tasks and we describe a brief proof of concept showing how Globus Compute could help to schedule jobs and be a tool to connect compute at different facilities.
We describe the deployment and use of Globus Compute for remote computation. This content is aimed at researchers who wish to compute on remote resources using a unified programming interface, as well as system administrators who will deploy and operate Globus Compute services on their research computing infrastructure.
Understanding Globus Data Transfers with NetSageGlobus
NetSage is an open privacy-aware network measurement, analysis, and visualization service designed to help end-users visualize and reason about large data transfers. NetSage traditionally has used a combination of passive measurements, including SNMP and flow data, as well as active measurements, mainly perfSONAR, to provide longitudinal network performance data visualization. It has been deployed by dozens of networks world wide, and is supported domestically by the Engagement and Performance Operations Center (EPOC), NSF #2328479. We have recently expanded the NetSage data sources to include logs for Globus data transfers, following the same privacy-preserving approach as for Flow data. Using the logs for the Texas Advanced Computing Center (TACC) as an example, this talk will walk through several different example use cases that NetSage can answer, including: Who is using Globus to share data with my institution, and what kind of performance are they able to achieve? How many transfers has Globus supported for us? Which sites are we sharing the most data with, and how is that changing over time? How is my site using Globus to move data internally, and what kind of performance do we see for those transfers? What percentage of data transfers at my institution used Globus, and how did the overall data transfer performance compare to the Globus users?
Developing Distributed High-performance Computing Capabilities of an Open Sci...Globus
COVID-19 had an unprecedented impact on scientific collaboration. The pandemic and its broad response from the scientific community has forged new relationships among public health practitioners, mathematical modelers, and scientific computing specialists, while revealing critical gaps in exploiting advanced computing systems to support urgent decision making. Informed by our team’s work in applying high-performance computing in support of public health decision makers during the COVID-19 pandemic, we present how Globus technologies are enabling the development of an open science platform for robust epidemic analysis, with the goal of collaborative, secure, distributed, on-demand, and fast time-to-solution analyses to support public health.
TROUBLESHOOTING 9 TYPES OF OUTOFMEMORYERRORTier1 app
Even though at surface level ‘java.lang.OutOfMemoryError’ appears as one single error; underlyingly there are 9 types of OutOfMemoryError. Each type of OutOfMemoryError has different causes, diagnosis approaches and solutions. This session equips you with the knowledge, tools, and techniques needed to troubleshoot and conquer OutOfMemoryError in all its forms, ensuring smoother, more efficient Java applications.
2. GenesisLab360, a laboratory information management
system (LIMS), the strongest and more flexible LIMS/LIS
Platform that is tailored not only to manage an
organization´s laboratory information but to provide an
integrated informatics solution and platform that allow for
outstanding laboratory capabilities for workflow
management, optimizing productivity and operating cost
with increasing quality.
3. GLab360 provides easy-to-use screens for physicians, IT employees, and laboratory technicians, to create the
configuration process with ease and have full control for simple and complex procedures ranging from test creation to
automatic verification rules.
Standards-Driven
Qualifications, role definition,
responsibilities, and equipment
resources. It also facilitates a
precise description of all phases of
testing, test validation. Planned
tests that are scheduled on a daily
or shift basis can be automated and
optimized.
The creation of master/reference
test plans and inspection schemes is
easy using GLab360. Thousands of
modifications in tests across the
board can be generated from a
single master with just a few mouse
clicks.
GLab360 Solution connects and
integrates laboratories with
production operations, regardless
of location. The solution optimizes
workflows from a centralized
testing platform. The system
interfaces and interoperates with a
broad variety of measurement and
test devices, including legacy
systems.
Automated and Easy Integration Lab-to-Line
4. GLab360 also provides a standard interface with HIS or ERP
systems for handling of master data and inspection orders with
feedback. A production order originating from the ERP system
can be imported, tested, and validated. The results can then be
fed back to the HIS or ERP system complete with observations,
recommendations, and specifically documented corrections.
A major advantage for the user is that the system is fully
developed, market-proven and ready to use. At the same
time, it has the flexibility to be customized to the specific
requirements of your environment. GLab360 will leverage
its expertise at every customer to optimize workflows and
ensure a fast and cost-efficient implementation. We help
you to create specifications to address your unique
challenges.
This information is very important for the next
user because the condition of the tool often
depends on the previous run process.
Logs give also hints for users regarding
parameters of standard and/or often used
processes. The tool usage history is a base for
planning and doing service and preventive
maintenance, i.e. no logs = no service!
Revolutionizes efficiency in LIMS implementations
Customized with Standards Fully Log System
5. Main Modules The user can easily operate between branches and departments
according to workload and pre-assigned privilege.
Home static
Dashboard
6. Registration
For patient data in a few steps, the user can either search and
choose a history patient or add new patient demographics.
Allowing configurations for mandatory field according to
customer needs.
8. Update Visit
Details
With just a mouse click, the user can update visit details with
the needed insurance companies, referral doctor.
9. Manage Whole
Visit Finance
The user can manage whole visit finance for any change or remaining
and payback with a full user log.
From one screen user can manage different tab to cover all the
mandatory and needed visit details for enhancing the result
verification process.
10. Unique Visit
ID generation
A Unique visit ID generation for each visit according to patient
ID.
Different visit status updated automatically to indicate
current visit progress
12. Sample Management
Our Web-based LIMS facilitates the
configuration of all checkpoints needed to be
routed during sample life cycle also with the
full web-based technique system can be
introducing and reviewed (from any mobile,
tablet, etc...) so now you can easily fully
control, update and guarantee your Sample
life cycle is following all the international
standards.
13. Glab360 is fully configured by
the user to choose for every
test the required sample type
and sample container.
Sample ordering
Process of sample physical generation
allows the user can easily submit the
collect order from the actual location of
collecting the sample from departments
to record the exact location and time for
sample creation
Sample collection & Barcoding
The unit is responsible for
collecting samples from different
locations and checking for
acceptance and validity.
Sample receiving unit
14. The system automatically sorts &
notify the Sample receiving unit user
with dispatching location needed for
different sample processing
Sample Dispatching:
A phase in which preparation
treatment for sample done according
to the needed criteria for analytical
processing
Sample preparation:
Process in which sample undergoes for
measurement through the instrument
which will be connected to our
Glab360 system using a set of various
stats of the art technology modules
Sample measurement:
15. The system will automatically update
the user for the sample expiry period
to be discarded, each according to the
pre-defined safety and ISO standards.
Sample storage Sample retrieval Sample Discard
Process in which the sample is
stored in a pre-defined location
with a pre-defined period of time
for any further needed work
Process of ordering a sample from the
storage location to the processing unit for
any needed further confirmation, or
result double-checked
18. Sample collection
Timestamp for every sample collected with the collection user.
Allow sample rejection in case of collection failure and clarify the
reason and rescheduling collection.
Different sample status that enables the technical lab users to be
updated with different sample stages.
19. Lab Module
Used to cover all technical lab work according to the worldwide laboratory
standards.
20. Instrument
Connectivity
Module
GLab360 system provides
- A bidirectional interface with the instrument
- Downloading all detailed information to the analyzer
- Monitor the connectivity status for your instruments
- Zero Footprint to help the lab utilizing any available space
21. Result reporting
Fully customized result reports according to customer needs.
Result reports will be available for printing only after validation which
ensures always accuracy and safety.
23. Dashboard
The Dashboard will be always updated with overall lab workflow
according to pre-configured Statistics per user with a full-screen view
24. Users will be fully engaged and controlled with the Dashboard.
Dashboard
25. Sample Tracking
Module
You will be able to track any of your samples for the last location and all
previous timing, processes, and users.
Support tracking samples between branches or internally in the
laboratory.
Support sending and receiving action for a sample.
26. Turn Around Time
module
You can easily calculate the turnaround time for any sample, visit or
average of a branch that gives you more capability for enhancing your
workload, throughput, control and fix any delay
27. Fully customized reporting
module to ensure that
customers' data always
updated and tracked with
financial and marketing reports,
for better and full control of
financial needs.
Fully customized statistics graphs
for better progress indication.
Claim module SMS moduleG-portal module
Allow patients to be always
connected to their results
history over the customer
website.
It can be configured to be used
by referral doctor or contracted
lab entities, insurance
companies to view results, order
visits and approved visits
requests.
Used to automatically send an
SMS to the patient including
encrypting data to view results
once validated by lab staff.
Also can be managed to send
SMS with the latest offers and
updates for the patient.
28. Provide an easy and monitored
way of communication between
all staff for following different
work processes and continuous
updates with the required tasks.
The system can be configured for
automatic user alerting in
different system modules
according to customer preset
criteria.
Allow lab users to configure
different criteria according to
the current test result,
previous, data check and other
related test formulas. To auto
validate and comment test
results.
Internal chatting module Alerting module Auto-validation module
29. Complete module to cover all the sent tests outside the lab starting from
pricing to final step of result entry including different lab range entry,
different screen for lab result entry, lab to lab worklist according to test
and activated lab and complete reporting with a related financial claim.
Lab To Lab module