Best Clinical Trial Management Software in Australia

The constructive IWRS ensures a well-organized, systematized supply of drugs between investigation sites. This reduces drug wastage and proactively handles complex randomization procedures for large multi-center studies. SyMetric Platform with Dynamic and Adaptive Randomization helps avoid imbalances between subjects. This results in balanced Treatment Assignment regardless of sample sizes. SyMetric Platform allows patients to handle their subjects. It offers Subject Screening and Enrollment as well as Visit Management, IP dispensing, receipt, Unblinding and Withdrawal tools. This makes it easy and efficient to manage them effectively. SyMetric Platform's robust IP supply management functionality allows drug supply mangers to closely control supplies sent to Sites and adjust supply strategies based on treatment arms and new ratios.

TrialPoint™, electronic data capture (EDC), is simple to set up and use. Coordinators love it. Our data managers are skilled in converting clinical protocols to geek-speak (metadata dictionary for those in the know). They will set TrialPoint™, so it works for you, and not against you. The system can accept any randomization string or media upload. It can blind users to treatment assignments. To promote time-sensitive data collection. The system will calculate visit windows and send reminders to keep the team on track. Many protocols are now being implemented in trial designs that include patient-reported outcomes on health and quality of life questionnaires. TrialPoint's electronic patient outcomes (ePRO), which can be configured to suit any quality of life questionnaire, patient diary, or other criteria, is worth a look.

Our market-leading solution for patient randomization, trial supply management, and patient randomization is available in multiple modalities. It is the most customizable and customizable Interactive Response Technology on the market. IXRS®, which is available in multiple modalities, can accommodate any combination of study objectives. It also includes a team of professionals biostatisticians, integration experts, and language experts that are available 24/7. Site-facing functions are designed for automating steps that are susceptible to human error. Site users can make data corrections themselves without having to call a Help Desk or fear of violating trial compliance. Instead of reading hundreds of pages of legalese and specifications, visual tools are easier to understand. You can view and react to every stage of the software build, eliminating surprises at delivery.

Protocol First bridges the physical distance and breaks down silos in Clinical Research during the pandemic. Our solutions can also be used for "normal times". Technology, once a luxury, is now a necessity. We offer the tools you need to stay connected. Not only to help you continue your research but also to speed it up. Remote monitoring and auto-tagging. It can be used with any EDC. Protocol First focuses on breaking down silos between Sponsors, Sites, CROs, and functional areas. We offer comprehensive solutions for the many problems in Clinical Research. Protocol First is focused on getting your data right and to the right places. This includes AI/NLP/ML, both today and in the future. Your data must have an underlying structure. This is the most important aspect of AI. Protocol First's software suite ensures that data from patient to FDA can be used to harness the power of data science.

Electronic source documents - eSource – eliminate paper, standardize and simplify workflow and reduce errors and omissions. BREEZE eSource does more than just schedule visits and create templates. BREEZE eSource synchronizes clinical contexts, regulatory requirements, and protocol requirements with study procedures. This ensures that users capture all protocol-required data. BREEZE business rules ensure that data collected is accurate, complete, accurate, and in compliance with regulations. Our dedicated team of clinical trial specialists delivers customized, study-specific eSource documents to review and approve before study start-up. They also support you throughout the trial by modifying them as necessary. Modules work seamlessly together. Cross-Module Action Multiplier takes things one step further, anticipating and completing automatically any additional tasks you enter. For example, the completion of visits or procedures automatically posts invoicing, recalculates scheduling, etc.

Maximize data quality. Capture eSource data during patient visits to ensure data quality. High-quality data can be electronically captured with built-in validation and edit checks. This reduces errors and queries and allows for remote monitoring. Study time, cost, and risk can be reduced. FDA approved eSource to streamline clinical trials. It eliminates slow, inefficient, and error-prone SDV and transcribing into EDC systems. Streamline study and site efficiency. ez-SourceDocx was designed with site users in view. It streamlines workflows, reduces workload, and ensures protocol execution. It guides sites through properly sequenced visits that guarantee all end points data and prompt quality investigator evaluation.

AI-powered medical image processing meets advanced clinical data automation. UNITY, available as a web-based SaaS solution or on-premises solution, is trusted by major medical equipment manufacturers and hospitals around the world to collect complete, compliant, and consistent data. The integrated modules for PROM and eCRF streamline key data collection to enable faster, more cost-efficient trials. RAYLYTIC’s Imaging Core Lab has decades of experience in high-precision, automated evaluation of musculoskeletal device performance and morphology in spine, hip and knee.

5thPort is an eConsent, patient engagement and digital education platform. It can be used in individual practices, hospitals, healthcare systems, and clinical research. The platform uses high-quality, prescriptive media and teach-back in order to educate patients and caregivers about their diagnosis, their care plans, the risks and benefits of recommended treatments, and more. Our digital eConsent helps facilitate a meaningful discussion with your healthcare provider once the patient has been informed. 5thPort can help you achieve the following: 1. Save 15 to 20 Minutes per consultation (without any additional effort) 2. Enhance the patient experience 3. Reduce patient anxiety on the day of their appointments 4. Encourage patients to actively engage in healthcare conversations with their providers 5. Reduce nurse burnout

Studypages is an integrated clinical trial management system designed to streamline clinical operations and unify participant experiences. It provides a set of tools to facilitate participant engagement, site administration, sponsor oversight, communications, collaboration, and workflow automatization. Studypages integrates these functionalities to create a single platform that increases the efficiency and effectiveness in clinical research. This accelerates the development of new medical innovations.

iOMS For Research Teams(c), was developed in collaboration by The Royal Wolverhampton Hospitals NHS Trust. It contains a cohesive integrated set of modules that helps all stakeholders effectively manage research management areas. All stakeholders can access a single platform that provides real-time views and engages them in research. Decision making is made easier by the inclusion of drill-down and detailed reports.

Ofni Clinical is a clinical database management tool that creates and quickly implements secure, regulatory-compliant clinical trial databases. Ofni Clinical offers comprehensive search and report capabilities, strong data validation and edit-check options, flexible customization tools, and is easy to implement quickly and economically. The databases can be used to collect data from existing Case Report Forms as well as electronic data capture systems that are paperless. Most Ofni Clinical projects take less than a month from project initiation to validation. Contact us today to learn more about Ofni Clinical and how it can be used for clinical trials. It matches your existing Case Report Forms, reducing training and implementation expenses while adding electronic data capture & review capabilities. Features include extensive edit checks and data validation to detect and correct data entry errors and support data analysis.

Octalsoft offers COTS packaged solutions services. This includes consulting, implementation, ongoing support, and maintenance. Octalsoft has been providing software solutions to power businesses for over 20 years. Our focus has remained the same: delivering exceptional customer service. You can outperform your competitors by embracing smart technology. Cloud computing can help organizations scale faster and grow quickly by embracing it. Octalsoft is a global IT outsourcing and consulting firm that offers extensive expertise in software selection, system integration, training, and ongoing support for software solutions based on web- and database technologies. We offer a variety of software solutions and IT Services to solve complex business problems. We help companies and organizations improve their processes and maximize their resources every day by providing strategic Information Technology solutions.

PATCHMASTERNEXT is an electrophysiological and electrochemical toolkit. It offers multi-channel stimulation and data collection with integrated online and offline analyses. PATCHMASTER NEXT can be used to drive amplifiers, including those with control features for EPC10 USB (Single-, Double-, Triple-, and Quadro). PATCHMASTER® NEXT can also manage surrounding components such as temperature controllers, perfusion system, and other devices. The most significant change you will notice when you first start PATCHMASTERNEXT is the modification in the graphical user interface. The new graphical user interface, along with the preserved workflow, should make it easier for existing and new PATCHMASTER users transition to PATCHMASTER. PATCHMASTER NEXT is a new version of the PATCHMASTER software. It represents the next step in the development of our patch clamp software.

The S-Clinica Anticipatory Management Engine powers the ClinVision suite. It is the most advanced algorithm in clinical supply planning, management and forecasting. The S-Clinica Anticipatory Manager Engine is the industry's most advanced algorithm for Clinical Supply Forecasting, Planning and Management.

Teckro clinical trial software connects all stakeholders to crucial information. Every time. Everywhere. Every day, we find answers from our smartphones. The same applies to clinical trials. Research staff and CRAs always have access to the most current study information. Research staff can access the most important details via their mobile devices by simply tapping a button. Site staff and monitors can be notified in real time if any updates or amendments are required. Teckro, a cloud-based clinical trial software that runs quickly and requires no installation, is quick and easy to set up. It's easy, intuitive, and simple. Teckro is secure hosted and in compliance with major industry regulations, such as FDA 21 CFR Part 11. You don't need to worry about version management as long as you have the approved version of the study documents.

All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to manage a clinical trial. All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to conduct a clinical trial that is successful. All aspects of your study can be covered with one platform. You can choose the app that you need in one environment, with no additional vendors or third-party.

eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.

Complete control. Full visibility. LifeSphere CTMS is an intuitive trial management system that allows clinical operations teams to reduce complexity, speed up timelines, and stay organized. A modern, user-friendly cloud application streamlines study management and automates key tasks throughout the trial's lifecycle. A simple yet powerful trial management app that gives full oversight of trial activities helps you navigate complexity. Streamline your clinical environment by using a turn-key platform that allows for payments and monitoring, and connects seamlessly with LifeSphere eTMF.

Leapcure, a leading platform for patient recruitment and engagement, connects clinical trial sponsors to eligible patients. We use advanced technology and strategies to improve patient outcomes and trial participation. Our platform streamlines recruitment, ensuring that suitable candidates are quickly and efficiently added to trials. Leapcure's mission is to advance medical research by making clinical trial more accessible and efficient. We work closely together with sponsors and patients in order to ensure a smooth and successful experience during the trial. This will ultimately contribute to the development of new therapies and treatments.