Alternatives to SyMetric
Compare SyMetric alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to SyMetric in 2026. Compare features, ratings, user reviews, pricing, and more from SyMetric competitors and alternatives in order to make an informed decision for your business.
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Medrio
Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM). Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services. Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating. -
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IQVIA
IQVIA
Thousands of organizations around the world trust IQVIA to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access to and delivery of healthcare, and ultimately drive better health outcomes. Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster. With a foundation in data, advanced analytics, and expert insight, IQVIA brings specialized capabilities to customers across the healthcare ecosystem. Read and watch the latest from IQVIA data scientists, doctors, researchers, and other subject matter experts on the topics that matter to you. From industry trends to how we are applying our capabilities to help, you can find it here. -
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ClinCapture
ClinCapture
At ClinCapture our mission is to build software that saves lives. Our technology lowers the cost of clinical trials by streamlining data capture processes while providing a platform that protects patient privacy. Clincapture advances the evaluation and development of drugs, biologics, and devices that demonstrate promise for the diagnosis and/or treatment of a wide range of diseases or medical conditions. -
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Clinion RTSM
Clinion
Using Interactive Response Technologies (IWRS), Clinion RTSM helps you with efficient patient randomization and clinical trial supply management The Randomization module of the Clinion RTSM Software allows you to implement simple to complex randomization strategies as per protocol specifications, fully integrated with Inventory. Clinion offers one of the most fully integrated EDC/RTSM platforms in the industry, so site users can perform Randomization and drug allotment, including returns and re-allotment, without having to log into two systems or worry about reconciliation Take advantage of our affordable and predictable pricing model to reduce the overall cost of RTSM ownership without sacrificing quality or functionality. Gain more by using our integrated EDC and RTSM modules -
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Randomize.net
Interrand
Unlimited trial duration, number of subjects, clinical sites, treatment arms and stratification variables, all for a one-time fee. Full support for double-blinded trials, including kit management, kit replacement and emergency unblinding. Randomize.net supports permuted blocked stratification, minimization and simple randomization algorithms. Configure randomization applications with the exact options and features you want. With Randomize.net's Web Service API, you can integrate randomization into your application. Full support for subject randomization and reporting available. Highly secure internet-based randomization service for clinical trials.Starting Price: $2,500 one-time payment -
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Ddots IDEA
Ddots
Standardized process for managing investigational agents to improve patient safety while maintaining regulatory compliance. Safeguards to prevent the selection of expired or quarantined agents when dispensing. Reduce the risk of dispensing to patients not enrolled in a study. Capture complete dispense details and record them in the DARF. Prevent the dispensing of drugs that will expire within the prescribed treatment period by evaluating the dispense date, supply amount, and expiration date. Track dispense details including drug thaw time, time of reconstitution, and temperature reading at the time of reconstitution. Centralized electronic management of investigational agents offers improved legibility, reduced paperwork/handwriting, and streamlined inventory management to provide pharmacists more time for valuable work and patient care. DARFs can be customized using filters yet still maintain a standard appearance for all protocols regardless of sponsor.Starting Price: $17,000 per year -
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Suvoda
Suvoda
Suvoda is a global clinical trial technology company specializing in complex, life-sustaining studies in therapeutic areas such as oncology, central nervous system disorders, and rare diseases. Founded in 2013, Suvoda offers an integrated platform that includes Interactive Response Technology (IRT), electronic Consent (eConsent), electronic Clinical Outcome Assessments (eCOA), and ePatient solutions, all designed to manage critical patient interactions efficiently. Their patented software architecture ensures a seamless user experience, facilitating precise randomization, drug supply management, and real-time data collection. Committed to enhancing patient comprehension and reducing site burdens, Suvoda's solutions are built to adapt to the evolving complexities of clinical trials. Headquartered near Philadelphia, with offices in Europe and Asia, Suvoda has supported over 1,500 trials across more than 85 countries. -
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Cenduit IRT
Cenduit
Today’s Interactive Response Technology (IRT) systems are increasingly complex. Flexible and configurable IRT matters - with IRT data as the source of record for recruitment, clinical trial drop-out rates, patient visits, and other crucial data. Choose a platform that’s user-friendly, mobile-ready, and comprehensive - embedded in quality, flexibility and expertise. Choose comfort with complex therapeutic expertise in today’s risk-based eClinical environment. Combining the right technology, subject matter expertise and commitment to service we empower clinical trials to deliver patient outcomes. Deep clinical and supply chain knowledge drives innovation and provides clients with control over their Randomization and Trial Supply Management (RTSM) processes. Our innovative suite of tools drives distinctive levels of quality control, site efficiency and patient compliance. Our IRT platform can meet the needs of almost any study, enabling fully validated deployment in as little as 30 days. -
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ez-DIMS
Alpha Clinical Systems
Drive study efficiency, regulatory compliance, and patient safety with Alpha Clinical Systems' electronic drug inventory management system (DIMS). Reduce site errors and workload while gaining real-time transparency. A comprehensive web-based system, ez-DIMS streamlines drug and device distributions at the site to eliminate transcription errors. Integrated with ex-SourceDocx, automatically accounts for supply disbursements, providing real-time visibility of drug inventory. Replace slow, error-prone, manual processes with user-friendly ez-DIMS. Reduce site workload with user-friendly scanners to quickly, easily, and accurately record study supply inventory and accountability at the patient, site, and study levels. Drug inventory violations at the site are the second most common regulatory inspection finding. Reduce medication assignment/dispensation errors by leveraging QC cross-checks between ez-DIMS and ez-SourceDocx. -
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Ennov CTMS
Ennov
Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers). Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible. - Comprehensive CTMS software - Integrated with Ennov Clinical Data Management - Clear visibility into investigational sites - Integrated workflow -
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Korio
Korio
Korio is the Randomization & Trial Supply Management (RTSM) platform designed for flexibility, quality, and speed. Not just built to tackle clinical trial challenges as they come, but built to prevent them in the first place. No matter what trials you may face, Korio is prepared to handle them. Legacy RTSM systems are not built to support the trend toward increasingly complex study designs. Brittle RTSM platforms do not easily accommodate on-the-fly RTSM design updates to match clinical trial changes. Inspired by decades of hands-on experience. The result is an RTSM platform where flexibility meets reliability, and modernity meets experience. Streamline your user experience with Korio's intuitive, role-based interface. From site users and supply managers to clinical operations and data managers, empower everyone to work faster and take action with confidence. Experience consistent management of your trial. -
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Pulse
Elevate Health Technologies
ElevateHT specializes in simplifying the intricate world of medical inventory, supplies, and drug management. Our solution, Pulse, transforms inventory and in-office drug dispensing into actionable insights, streamlining your processes and empowering you to make informed decisions. With us, managing your inventory becomes effortless, allowing you to devote your energy where it truly matters – providing exceptional patient care. Our cloud-based system facilitates simultaneous real-time transactions, enabling multiple users to conduct operations swiftly. With its scan in, scan out functionality, it offers both convenience and security, ensuring accurate recording and user attribution. Enhance product tracking and patient records by monitoring items via their serial and lot numbers. Anticipate product expiry to avoid wastage and facilitate lot recalls when necessary.Starting Price: $250 per month -
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TestVault
TestVault
This is software so simple that you'll barely need customer support, but when you do, we're always here to help. This is TestVault, the most advanced and user-friendly drug testing software on the market. Whether you're running random selections, generating DOT MIS reports, or just trying to get your invoices out the door at the end of the month, TestVault is there to help you every step of the way. We've spent years listening to feedback from hundreds of TPAs, MROs, collection sites, and other drug testing companies. And we've used that guidance to build the first drug-testing software that is truly easy to use. Sign up for a demo today to see how much easier managing your drug testing business could be. -
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IXRS®3
Almac Clinical Technologies
Available in multiple modalities, our market-leading solution for patient randomization and trial supply management is the most configurable and customizable Interactive Response Technology available. From Phase I through to IV, simple designs to complex adaptive trials, IXRS®3 will easily accommodate any permutation of study objectives, and with it comes a team of professional biostatisticians, language and integration experts who are at the ready 24/7. The site-facing functions are designed to automate steps that are prone to human error. Site users have the freedom to make data corrections without the need to call a Help Desk for support or fear of deviating from trial compliance. Easy-to-read visual tools instead of hundreds of pages of specifications and legalese. View and react to each stage of the software build along the way, eliminating delivery surprises. -
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DrugDev Spark
IQVIA
DrugDev Spark™ is the world’s first comprehensive unified clinical operations suite. Explore our solutions below to learn why so many sponsors (including 9 of the top 10) and CROs (including 4 of the top 5) trust DrugDev technology. DrugDev Spark™ is the industry’s first comprehensive unified solutions platform – comprised of innovative technology and expert services proven to add value on thousands of clinical trials. From planning through closeout, our solutions are rigorously tested and improved by sponsors, CROs and sites of all sizes, in more than 60 countries. Through this experience, we have established and integrated best practices into every feature of our system. That’s why 9 of the top 10 pharma, 4 of the top 5 CROs, and the biggest industry collaborations are among the many organizations that trust DrugDev technology. Most of the world’s top sponsors and CROs are using DrugDev solutions to transform how they run clinical trials through collaboration. -
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ElevateHT
ElevateHT
Pulse, developed by ElevateHT, is a cloud-based medical inventory management solution tailored for clinics to streamline the handling of medical supplies and drugs. It offers real-time inventory tracking with scan-in, and scan-out functionality, ensuring accurate recording and user attribution. The system enables monitoring of lot and serial numbers, as well as expiration dates, to prevent wastage and facilitate efficient product recalls. Pulse's intelligent purchase planning allows for setting custom order points and provides usage-based suggestions to optimize stock levels, ensuring adequate supplies for patient appointments. Automated reporting features deliver detailed insights into tracking, order evaluation, and profitability, with options to schedule reports as needed. Integration capabilities with suppliers, Practice Management Systems (PMS), and Electronic Health Records (EHR) enhance productivity by reducing the need to navigate multiple systems. -
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HelioMetrics
HelioMetrics
Diversion of controlled substances can occur anywhere in the pharmaceutical supply line, but more predominantly in hospital pharmacies and healthcare delivery. HelioMetrics Healthcare Rx Drug Diversion Analytics Software can help speed up identification of drug diversion activity, accelerate your diversion investigations and reduce associated drug diversion costs in healthcare. Look in the news and you are sure to find something about the “opioid epidemic” and how there are problems everywhere with healthcare workers and pharmacists stealing these and other drugs. In some cases, the healthcare worker has even caused HIV and Hepatitis C concerns. Some of these cases have moved into the legal world with hospitals facing hundreds of lawsuits from former patients. Not to mention the fines that the DEA is now handing out. The risk of drug diversion is real, not only from a patient safety issue, but from financial issues for the healthcare facility. -
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PharmCare SaaS
PharmCare Technology Limited
PharmCare SaaS is a Community Pharmacy Solution with Patient Record / Drug Review Management, Prescription Management, Medication Record / Stock Management and Dispensing / Drug Label Management which support multi-branches / outlets, multi-languages, Drug Icon CC support. -
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TCS ADD
Tata Consultancy Services
TCS ADD platform accelerates speed-to-market for pharmaceutical industry across the entire clinical R&D value chain and helps make clinical trials more agile and safe. TCS ADD enables digital ecosystems, simplifies data complexity and provides faster access to new and effective drugs for the patients. The platform is powered by cognitive artificial intelligence engine called TCS Decision FabricTM, smart analytics and IoT that provides superior business value to pharmaceutical industry. A next-generation and end-to-end metadata-driven solution to manage industry & sponsor clinical standards. A data science-driven platform that leverages AI & ML technologies to enable quicker decisions, faster study start-up and targeted interventions. A solution that digitizes the entire clinical trial supply management process while putting the patient in the center, increasing patient’s safety and overall efficacy. -
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Oracle Clinical One
Oracle
Clinical One RTSM can support a randomization strategy for the simplest to the most complex studies without the need for programming or coding, which eliminates the need for prolonged user acceptance testing. Take control of your study through self-service configurations and build a study in days instead of weeks. Assess the status of the drug inventory and make modifications in real-time without reverting to the vendor and incurring cost and change requests. Eliminate change request costs and avoid delays by quickly implementing changes and promoting your studies in seconds. The only platform that truly unifies people, processes, and data to simplify and accelerate the clinical trials of the future. Virtual components in clinical trials allow greater patient participation and significantly improve clinical trial data quality. Transformative digital strategies are needed for faster study startup to harmonize data from any source and to streamline workflow. -
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Protocol Manager (CTMS)
Atlant Systems
Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development. When the appropriate Standard Operating Procedures (SOPs) are implemented in your company, Protocol Manager can help you be compliant with the FDA’s 21 CFR part 11 regulations. Protocol Manager supports Web Services technology to provide seamless, automatic integration with many popular EDC and IVRS products. For systems not supporting Web Services, integration is supported via an export/import mechanism. A robust tracking tool and database designed to manage myriad trial information and metrics. -
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eCaseLink
DSG
DSG, Inc. is a leading global eClinical provider with a fully unified suite of innovative technology solutions and data management services for the global clinical research community. DSG's eClinical software platform provides competitive advantage that is cost-effective with on-time project delivery. DSG solutions have been used in thousands of clinical trials around the globe with our award-winning eCaseLink™ platform and eCaseLink Designer for enterprise licensing. Founded in 1992, the company is proud to be recognized as the first provider of a fully integrated EDC and IRT Randomization and Trial Supply Management system with the SCDM Data Driven Innovation Award. -
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Agilum
Agilum
We enable the leap to value-based care by comparing treatments, drugs, processes, and costs to help hospitals, life science companies, and payers identify treatment plans that achieve the best patient outcomes. Our CRCA™ P&T platform empowers P&T committees to yield data-driven improvements in quality metrics, such as average length of stay (ALOS) and 30-day readmissions. Our unique POP-BUILDER Rx™ solution provides comparative analyses between selected cohorts and CRCA’s real-world data index of over 140MM longitudinal patient records. Our drug remittance dashboard analyzes and reports drug remittance data across payer types and for focused groups of high-cost drugs down to the NDC level. We help hospital finance departments quickly and easily monitor and improve service line costing and profitability, productivity, and revenue cycle performance via insightful analytics, reporting, and our Agilum Healthcare Intelligence team. -
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DrugPak
DrugPak
DrugPak’s client portal add-on provides the opportunity for you to create a company-branded dashboard for your clients. Once logged in, your clients can access their information in a secure environment. In the portal, they can view reports (new and historical), view random profiles, add participants individually or in a bulk upload, and manage their company data (authorized contacts, employee lists, and locations). DrugPak’s Notification/Dashboard provides instant access to your most important metrics and common actions. The dashboard can show common metrics used by your company, which may include such widgets as expiring licenses, expired licenses, expired physicals, login activity, DOT, and Non-DOT. Dashboard widgets can be created to meet your needs when our custom programing services are utilized. -
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Clinical Concepts
IVR Clinical Concepts
IVR Clinical Concepts specializes in providing virtual clinical trial technology and patient engagement solutions. Their offerings include electronic patient-reported outcomes and patient diaries, which aim to deliver better data with fewer errors, resulting in shorter timelines and lower costs. They also provide patient recruitment and outreach services, focusing on outreach, pre-screening, and real-time data collection. Their subject screening, registration, and randomization solutions are described as modular, custom, flexible, and configurable. Additionally, IVRCC offers clinical trial material management solutions designed to reduce workload while providing more control, as well as eClinical integration services to seamlessly thread data together. Their chart review services provide real-world data and clinical insights. IVRCC emphasizes custom, modular, and configurable solutions to improve the patient experience and optimize clinical trial success. -
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ePharmaSolutions
ePharmaSolutions
At ePharmaSolutions, we are building something new. We are not a high-tech company. We are an idea company whose thinking is highly entrenched in technology, but not limited by it. We support the drug development industry with solutions that improve the identification, activation, training and management of clinical trial sites. With new perspectives on old problems, we deliver technology-enabled solutions that help to “un-complicate” the chaos of clinical trial management. ePharmaSolutions (ePS) is a leading provider of e-clinical solutions that improve the way that clinical trial sites are selected, trained, activated, and managed. By applying fresh thinking to old problems, we deliver clever, technology-enabled solutions that empower sponsors, contract research organizations and investigator sites to “un-complicate” the chaos of clinical trial management. -
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Zelta
Merative
Zelta is a cloud-based unified clinical data management and acquisition platform with adaptable modules that can be tailored to meet the unique needs of your clinical trials program and accelerate outcomes. It offers features such as electronic data capture, clinical operations tools like randomization and trial supply management, clinical trial management system, electronic trial master file, and patient and provider engagement solutions including electronic clinical outcome assessments and electronic consent. Zelta is designed to manage clinical studies across all phases, therapeutic areas, and regions, providing a user-friendly interface and seamless access through single sign-on from anywhere in the world. The platform emphasizes flexibility and scalability, allowing for customization to align with specific study goals and the integration of solutions from both Zelta and other technology vendors. -
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Arone
Arone
With over 20 years of experience in both software edition and clinical research sectors, Arone provides clinical research organizations with a complete suite of tools for patient data entry and management. Our solutions are turnkey and our team provides you with personalized support for the proper conduct of your projects and studies. Collect and manage patient data in a single tool. Arone manages the randomization of patients by randomly assigning study participants a type of treatment in order to remove bias in the study. Empower participants of clinical trials for their daily data entry. Benefit from a customized support for your projects. -
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Cloudbyz Safety & Pharmacovigilance Solution is a cloud-based software solution designed to streamline the drug safety and pharmacovigilance operations for pharmaceutical and life science companies. The solution helps to automate the process of collecting, processing, analyzing and reporting adverse event data in compliance with global regulatory requirements. Cloudbyz Safety & Pharmacovigilance Solution enables companies to reduce risk, improve compliance, and enhance patient safety while accelerating drug development. Cloudbyz provides end-to-end management of the pharmacovigilance lifecycle, including adverse event processing, case management, regulatory reporting, signal detection, and risk management. With Cloudbyz, you can optimize your pharmacovigilance processes, accelerate case processing, and increase the accuracy of your safety data, while minimizing risk and ensuring compliance.
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Healnet
Healx
Rare diseases are often not well studied and there is a limited understanding of many of the aspects necessary to support a drug discovery program. Our AI platform, Healnet, overcomes these challenges by analyzing millions of drug and disease data points to find novel connections that could be turned into new treatment opportunities. By applying frontier technologies across the discovery and development pipeline, we can run multiple stages in parallel and at scale. One disease, one target, one drug: it's an overly simple model, yet it's the one used by nearly all pharmaceutical companies. The next generation of drug discovery is AI-powered, parallel and hypothesis-free. Bringing together the key three drug discovery paradigms. -
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Paracelsus
Advanced Computer Technologies
Paracelsus has tools to help you effectively manage your drug testing program with timely test results. It provides an easy to use, intuitive means to enter data, generate orders and retrieve results quickly and easily. All the criteria needed to run a full lab are available; chain of custody/requisition documentation, bar coding (used to integrate with drug testing analyzers), multi-tiered hierarchy, random color code scheduling, online reports, and the ability to invoice agencies and sub-agencies. Paracelsus is an inexpensive way to control your drug testing needs and perform accurate drug testing for your customers. Screening analyzers currently supported include: Indiko, Indiko Plus, MGC240, Biolis 24i, Biolis 50i, VIVA-E, VIVA JR., VIVA TWIN, Beckman (Olympus); AU2700, AU400, AU480, and AU640. Confirmation analyzers (manufacturers) currently supported include: AB Sciex, Agilent, and Thermo Fisher. -
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AarogyaAI
AarogyaAI
We are an artificial intelligence-enabled SaaS that diagnoses drug-resistant tuberculosis in a few hours. AarogyaAI aims to diagnose drug-resistant tuberculosis (DR-TB) using Artificial Intelligence in a few hours. We enable quick and accurate diagnosis of DR-TB so that the patient can be rightly prescribed effective drug combinations for treatment, instantly. Tuberculosis claims more lives every year than AIDS. This is because, of the 19 anti-TB drugs available, doctors don’t always know which ones will work for whom. Thus, even though tuberculosis is curable, a delayed diagnosis of drug-resistant tuberculosis can mean patients are on ineffective medication for up to 7 years. AarogyaAI aims to diagnose drug-resistant tuberculosis in a few hours so that a patient can be prescribed effective treatment, instantly. We use a DNA sequence from the patient which is uploaded to our SaaS. Our machine learning algorithm then gives an output report of a comprehensive drug susceptibility status. -
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HealthEase
CSM Technologies
From making Primary Health Centers more efficient to building a robust supply chain for medicines and medical equipment to making hospital administration easy. CSM’s Healthcare Solutions have been at the forefront of making it easy for both governments by helping them manage their health centers better to large corporate hospitals by ensuring the system runs like clockwork. - Community Health Worker System - Drug Distribution & Supply Chain System - Hospital Administration Management System - Scheme Monitoring System -
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mIRT
DDi
Optimize clinical trials with our advanced RTSM clinical supplies software. Experience seamless clinical trial supply management with smart automation-driven forecasting, real-time tracking, and cost-efficient solutions. Request a demo today! -
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ClinVision
S-Clinica
The ClinVision suite of integrated modules is powered by the S-Clinica Anticipatory Management Engine is the most advanced algorithm in the industry for Clinical Supply forecasting, planning and management. The S-Clinica Anticipatory Management Engine is the most advanced algorithm in the industry for Clinical Supply forecasting, planning and management. -
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RxConnect
Netsmart Technologies
RxConnect is a web-based pharmacy solution specifically designed to meet the medication dispensing needs of inpatient hospitals. Its easy-to-use interface allows clinicians to send pharmacy orders directly within their EHR, electronically connecting order entry with pharmacies to seamlessly receive and provide medication. RxConnect supports dispensing capabilities with automated dispensing machines (ADMs) and connects with the electronic medication administration record (eMAR) to provide closed-loop medication management. Clinicians can review and manage drug interactions, allergies and patient-specific dosing via a clinical rules engine. Drug disease, alcohol interactions as well as lab and tobacco, pregnancy, lactation and general precautions and black box warnings are also provided. Inventory, formulary, progress notes, labs integration and intervention documentation, as well as pharmacy notes, are all included. -
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PolyDIS
HopitalWeb
PolyDIS: The electronic medical record for the GH (General Hospital), MCO (Medical/Surgery, and Obstetrics), Ehpad (Long Term Care Sector), HAH (Hospital At Home) . PolyDIS is the ideal patient management tool for public or private health care institutions, regardless of the activity: MCO (Medical/Surgery, and Obstetrics), Ehpad (Long Term Care Sector), HAH (Hospital At Home), SSR (Follow-up Care and Rehabilitation), Psy, etc. Revolving around the electronic medical record and integrating the electronic care record, nominative drug dispensing (CBUM or Contract for good (drug) practices), the recording of medical procedures and treatments, nursing, and sterilization, PolyDIS offers you the traceability everybody in the healthcare industry is looking for! PolyDIS secures the patient's path in the establishment, links and federates the departments. In operation since 2005 (with complete availability!) and regularly upgraded according to user establishment needs,PolyDIS is now a "field" -
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DTSMS
Btwixt
Vendor-provided database and software resources to store, manage, and protect a projected volume of thousands of drug testing records. The system and interfaces, if applicable, must contain HIPAA-compliant security to protect content, user, and protected health information data. This security system must maintain a secure set of user privileges, which determine permission levels that users need to control, manage and update content. Must allow for different county agencies to utilize the same software with the ability to provide random drug testing support to multiple agencies/groups and the ability to configure each agency independently.Starting Price: $25 per year -
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SupplyNote
Adcount Technologies
SupplyNote is a web-based supply chain management platform designed to help restaurants and cloud kitchens in the Indian market manage inventory, orders, employees, and customers on a centralized platform. Features include resource planning, order history tracking, reporting, payment processing, and sales performance metrics. The application enables restaurateurs to search, purchase, and interact with sellers, manage seller-wise ledgers, and track cash flows with real-time accounting. With SupplyNote, users can record inventory details such as product name, SKU, and quantity. Managers can gain insights about low-stock items and control inventory wastage or pilferage. It also lets users automatically create carts based on sales, wastages, or recipes. SupplyNote provides recommendations on sourcing, distribution, and operations based on the cost infrastructure of the business. Staff members can prepare new purchase orders with vendor name, pick-up and drop-off locations, date, billStarting Price: $300 per year -
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Quva BrightStream
Quva
Quva BrightStream is a cloud-based intelligence platform designed for health-system pharmacy operations that aggregates, normalizes, and integrates clinical and operational data across all sites of care to deliver quantified and prioritized insights. It includes AI- and machine-learning-driven modules such as Shortage Navigator (predictive supply-chain shortage detection), Diversion Surveillance (drug-diversion monitoring), Supply Advisor (aligning inventory to patient demand), Script Revenue Capture (identifying prescription revenue leakage), Contracts Value Maximizer (ensuring contract compliance and price-performance), and Clinical Process Optimizer (order-set, formulary, and protocol management). It supports senior leadership dashboards offering one “single pane of glass”, while enabling drill-downs into prioritized opportunities such as cost reduction, inventory optimization, diversion control, and revenue growth. It claims proven community results. -
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RealTime-CTMS
RealTime-CTMS
RealTime-CTMS is a premier, cloud-based clinical trial management system (CTMS) purpose-built to boost efficiency and profitability for site networks and research sites. Comes with fully-integrated services that include RealTime-PAY, RealTime-TEXT, and RealTime-eDOCS (the first fully-integrated eRegulatory document management system), the solution promotes quicker and easier access to subject or study information using simple and intuitive navigation. RealTime-CTMS offers a host of other solutions that covers online document storage, appointment reminders, data collection, payment processing, among others.Starting Price: $295.00/month -
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Saama
Saama
Actionable insights, driven by the industry's #1 AI-powered clinical analytics platform, enable your teams to manage risk and improve performance across studies, systems, sites, and vendors. State-of-the-art clintech from Saama is designed to streamline your workflows, automate time-consuming processes, and improve collaboration across clinical operations, medical review, data management, biostatistics, and pharmacovigilance. Sponsors and CROs rely on Saama for data aggregation and artificial intelligence solutions that lead to better decision-making, eliminate delays, and significantly shrink drug development costs and timelines. Saama can put you on the fast track to clinical trial process innovation. When all your clinical data is in one place and updated in real time, life’s much easier for your ClinOps and medical review teams. Data Managers have been underappreciated for too long. Eliminate manual work so they can pay attention to the data points that matter. -
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TrialPoint
Databean
TrialPoint™ electronic data capture (EDC) is easy to configure, easy to use, and the coordinators love it. Our data managers are experts in converting clinical protocols into geek-speak (metadata dictionaries for those in the know) and will configure TrialPoint™ to work for you, not against you. The system can accept any randomization string, media upload, or coding dictionary. It can even blind users to treatment assignments. To promote time-sensitive data collection. the system will prospectively calculate visit windows and send out alerts and reminders keeping the team focused and on task. Nowadays, patient-reported health outcomes and quality of life questionnaires are included in most trial designs and are responsible for many protocol compliance issues. Take a look at TrialPoint’s electronic patient-reported outcomes (ePRO) module which can be configured to fit any quality of life questionnaire or patient diary. -
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SimpleTrials
SimpleTrials
SimpleTrials is an on-demand, subscription-based Clinical Trial Management System (CTMS) designed for sponsors, Contract Research Organizations (CROs), and investigative sites. It offers a comprehensive suite of tools to effectively plan, manage, and track clinical study portfolios, including features such as site startup and subject tracking, document management with integrated electronic Trial Master File (eTMF), real-time study analytics, calendar and monitoring, custom fields and trackers, ad-hoc reporting, planning and milestones, site contracts and payments, and electronic visit reports. It supports compliance with 21 CFR Part 11 and provides a secure, validated environment for clinical trial data. Users can customize tracking views, integrate with various Electronic Data Capture (EDC) systems, and utilize built-in templates for consistent document management.Starting Price: $849 per month -
45
SiteCentric
SiteCentric
SiteCentric is a unified clinical trial management platform built by research sites for research sites, consolidating CRM, eISF, CTMS, finance, and reporting into a single system. It standardizes and automates workflows across the entire trial lifecycle, nurturing study leads and organizing pipeline activity with a purpose-built CRM; centralizing budgets, contracts, eReg, training records and source documentation for rapid startup; boosting enrollment through targeted outreach and querying existing databases; tracking patient visits and capturing high-quality eSource data; running internal QC checks, version control and audit-ready eISF documentation; managing budgets, invoicing, payment reconciliation and patient reimbursements; and delivering leadership dashboards to uncover performance metrics and trends. -
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Automizy
Automizy
Automizy is an Email Marketing Automation software. We offer AI-powered Subject Line Tester, AB testing, Resend, and Email Automation. Features made to increase your email open rate by 34%. Automizy provides you with tools to make your emails stand out in a crowded inbox. You can also, send campaigns, build automation, create forms, manage contacts, measure and optimize results. Write up to 4 different subject lines for your automated emails. Our multi-armed bandit algorithm optimizes and sends the variations with the highest open rates.Starting Price: $9.00/month -
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S2K Pharma
VAI
The pharmaceutical industry experiences ongoing changes. The challenges of increased market demand and stricter legislation increases the demand for more efficient and flexible supply chain management solutions for pharma distribution companies. VAI’s S2K Pharma OnCloud software utilizes advanced technology to help you meet those challenges head-on, as well as to improve operational processes and to monitor and collect data for reporting to drug enforcement agencies. Automation in the pharmaceutical supply chain is critical to ensure success. Leveraging 40 years of enterprise management software experience, S2K Pharma OnCloud is a completely integrated ERP software solution that helps pharmaceutical companies ensure that industry-specific regulations and institutional requirements are met, while helping companies lower costs and increase customer satisfaction. -
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Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.
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CORE (Clinical On-demand Research)
CIRU, University of Southampton
CORE (Clinical On-demand Research) covers a range of expert services which include the design, build and running of electronic forms used in clinical trials across the UK and overseas. Not only does CORE create the forms you need, it also offers randomization, data management and provides you with those all-important study statistics. CORE captures vital data for researchers working both in the academic world and commercial setting. CORE has developed a fruitful partnership with FormsVision, which the Unit first engaged with under a FP7 EU funding framework, and has successfully deployed the ALEA eCRF (electronic Case Report Form) to support trials within the UK and New Zealand. The CORE team offer a range of services which include: Database build. (CRFs, randomisations, drug supply management and ePRO (ALEA)). Data hosting (ALEA hosting for data/videos/images/documents). Expert advice (including funding application, statistics support and writing a protocol advice). -
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Prescription Pad
CompuRx Infotech
Safe, first-rate, foolproof prescription writing facility. Comparative Analysis Of Patient's Medical History. Check Drug Interaction & Brand Interaction. Automatic drug safety checks. Enables searching suitable drugs & brands. Keep record of every visit of individual patient in chronological order. A new Prescription would take even less than 2 minutes to complete. Scan patient's past history, family history and give you useful tips. Check for drug safety at individual disease level also like in case of G6PD, PORPHYRIA, HYPERTENSION, COPD etc. Makes the life of both the doctors and patients easy, comfortable and organized. Complete prescribing information of nearly 70,000 Brands of Indian, British & American drug database Pharmaceuticals. Full monograph of nearly 3,000 drugs (generic drugs) compiled from PDR of U.S.A., Martindale book of pharmacology, British National Formulary etc. Contains complete diagnostic information, differential diagnosis & treatment protocols.Starting Price: $170 one-time payment