Innovate Your Research
Innovate Your Research
Achieve unparalleled efficiency, reproducibility and study result quality with Seralogix Study Manager™—integrating statistically rigorous experimental design, seamless electronic data capture, and comprehensive reporting to ensure every study meets the highest scientific standards.
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Designed to elevate every phase of your study workflow, the Study Manager connects Study Organization, Experimental Design, Electronic Data Capture, Reporting, Team Collaboration, and your built-in Personal Assistant into one seamless, guided experience. From planning and powering your study with statistical rigor, to capturing high-quality data, to generating compliant reports and keeping your entire team aligned, Seralogix delivers a cohesive platform that enhances reproducibility, efficiency, and confidence in your scientific outcomes. Discover how a unified workflow can transform the way your research team designs, conducts, and communicates its work.
Welcome to Seralogix Study Manager™, the all-in-one platform designed to standardize and simplify preclinical studies like never before. With an intuitive, powerful interface, this platform is built for everyone from independent researchers to expansive research teams, providing the tools and flexibility needed to streamline your entire research process.
The Study Organizer provides a streamlined view of all research projects organized by investigator, program, or institute, enabling users to create and track the status of studies with ease. Instantly see which projects are in the design phase, active in data collection, ready for reporting, or completed. This role-based tool empowers administrators, program managers, technical staff, principal investigators, and invited guests with tailored access to key project information, ensuring efficient study management and enhanced collaboration across teams.
Instantly view all studies by investigator, program, or institute for complete operational visibility.
Administrators, program managers, PIs, technical staff, and invited guests get tailored permissions for secure, efficient collaboration.
Quickly identify which studies are in design, collecting data, ready for reporting, or completed—keeping teams aligned and proactive.
Program managers and administrators gain a high-level view to monitor workload, resource needs, and study timelines.
Program managers and administrators can create teams, assign roles and permissions, and send invitations to internal and external collaborators.
The Experimental Design Module enhances the setup process, making it easy to initiate new projects—whether starting from scratch, using a template, or building off a previous study. With just a click, you can begin defining your study, guided step-by-step through creating a robust experimental design. This intelligent module calculates optimal sample sizes and recommends the most appropriate statistical methods for your specific study goals. By offering the flexibility to explore different design options, it empowers researchers to craft precise, reproducible study protocols that enhance data quality and ensure statistical rigor, all while saving valuable time.
Create new designs from scratch, templates, or prior completed studies.
Configure groups, conditions, treatments, blocking factors, and outcome response variables.
Access thousands of pre-measured phenotypic responses for effect size estimation.
Define user-specific outcome metrics when needed.
Automatically recommends appropriate statistical models based on design parameters.
Computes required sample sizes using target power and significance levels.
Handles a multitude of study types that include crossover, parallel, randomized design, randomized block design, factorial designs, repeated measure designs, and blinded/unblinded.
Builds an event timeline specifying treatment, dosing, sampling, and observation points; supports time-based or condition-dependent triggers with system-generated event IDs.
Finalized designs automatically generate data collection frameworks.
Simplify your research process with Seralogix Study Manager’s Data Collection module, designed to automatically create a data framework based on your experimental design. Once your design is finalized, the platform ensures seamless subject enrollment, precise data capture, and adherence to study guidelines—all in one integrated system.
Dynamically constructs a complete data collection schema directly from the finalized experimental design, including subject groups, treatment schedules, measured outcomes, and longitudinal event structures.
Easily import partial or complete data from existing spreadsheets.
Executes fully automated randomization sequences with support for stratified, blocked, or restricted randomization; generates blinded role assignments and treatment masking metadata.
Provides controlled subject enrollment workflows with enforcement of inclusion/exclusion rules, stratification requirements, cohort balance constraints, and unique subject identifier generation.
Builds an event timeline for data collection scheduling based on the Experimental Design defined timeline events.
Issues real-time notifications for upcoming, due, late, or missed collection events; logs time stamps for audit and compliance tracking.
Enables distributed data entry with device-agnostic web forms; supports secure multi-site access, metadata tagging, and audit-trail recording for all data entries.
Automatically constructs electronic CRFs based on protocol-defined variables, measurement types, units, ranges, and controlled vocabularies.
Performs real-time validation against numeric ranges, categorical constraints, missing data rules, and protocol-defined logical dependencies.
Stores all captured data in a secure, multi-redundant architecture with encryption in transit and at rest, versioning, and recovery capabilities.
The Reporting Module generates complete, protocol-driven reports at every stage of your study—from experimental design and subject enrollment to data collection status, statistical summaries, ARRIVE compliance, and SEND 2.1–formatted outputs. With automated, standards-ready documentation available at a touch, you can accelerate reviews, streamline submissions, and ensure transparent, reproducible reporting.
Produces structured reports detailing study groups, conditions, treatments, environmental variables, outcome measures, event timelines, and sample size derivation based on power and significance criteria.
Generates enrollment summaries including stratification details, cohort balance, inclusion/exclusion application, and randomization assignments
Creates a detailed, time-indexed schedule of all treatment and measurement events, including event identifiers, timing rules, and procedural dependencies.
Provides dynamic dashboards and exportable reports showing completed, pending, late, and missed collection events with time-stamped audit records.
Executes summary statistical analyses (e.g., distribution metrics, variance estimates, outlier detection flags) based on the defined experimental design model.
Auto-populates a structured compliance matrix aligned with ARRIVE reporting standards, covering design transparency, methodology, and result reporting requirements.
In Development: Generates SEND 2.1–formatted output with standardized domain structures, variable sets, and controlled terminology mappings.
Supports export to PDF, CSV, Excel, and JSON formats for downstream analysis, archiving, or regulatory submission workflows.
Embeds study metadata, protocol identifiers, version history, and audit-trail elements into each generated report.
The Team Module enables seamless, role-based collaboration across your entire research workflow. Assign permissions, coordinate study activities, exchange feedback in real time, and keep every team member aligned with automated alerts and shared access to designs, data, and reports—whether your collaborators are across the lab or across the globe.
Defines granular permissions for administrators, principal investigators, program managers, reviewers, and data-entry personnel.
Supports secure user provisioning, credential controls, session management, and audit-logged access events.
Provides shared access to study designs, collection plans, reports, and status dashboards with version-controlled updates.
Dispatches automated notifications for design finalization, enrollment actions, data collection events, delays, and pending tasks.
Records user actions, role assignments, data edits, and report generation events for compliance and traceability.
Allows distributed teams to access synchronized data and workflow components with consistent permissions across institutions.
Facilitates controlled sharing of study artifacts, analysis files, and exported reports within defined permission boundaries.
The Expert Personal Assistance Module delivers intelligent, on-demand guidance throughout every stage of your study workflow. Powered by integrated AI (in development), it answers questions about platform functionality, assists with statistical concepts, provides explanations of study design principles, and helps interpret reporting outputs. With contextual insights, task reminders, and proactive suggestions, it acts as your always-available research companion—enhancing productivity, clarity, and confidence in your scientific decision-making. Included in this module is traditional creation of user trouble tickets and resolution status.
Provides natural-language responses to user questions related to platform functionality, study workflows, module operations, and system behavior.
Delivers explanations of statistical concepts, model selection logic, power analysis principles, and reporting interpretation within the context of the active study design.
Tailors guidance based on the user’s current module, study state, design parameters, or data collection progress for targeted and relevant support.
Helps translate study protocols into structured design components, variable definitions, and collection schedules.
Identifies common configuration errors, missing parameters, inconsistent design factors, or data validation issues and recommends corrective actions.
Offers contextual training, how-to explanations, glossary definitions, and best-practice recommendations to support new or advanced users.
Maintains audit-trail records of assistance queries, system suggestions, and user-triggered actions for transparency and compliance monitoring.
Seralogix Study Manager is designed and customizable to support a wide range of research organizations—from academic labs and biotech startups to CROs and global pharma teams. Explore how the platform adapts to the needs, scale, and workflows of each customer type.
You’ve seen the features—now discover how Seralogix can streamline study workflows, reduce administrative burden, and support reproducible research across your lab or department. Explore more to see how the platform empowers faculty, trainees, and collaborative teams alike.
You’ve seen what each module offers—now learn how Seralogix integrates seamlessly into large-scale research environments, enhances data integrity, and supports complex, multi-phase studies. Explore further to understand how the platform strengthens decision-making and accelerates discovery pipelines.
You’ve explored the capabilities—now see how Seralogix can accelerate your R&D, support lean teams, and provide the infrastructure needed to scale. Continue on to discover how a unified platform helps startups grow faster with confidence and scientific rigor.
The modules you’ve reviewed are designed for high-throughput, precision, and client-ready documentation. Dive deeper to see how Seralogix enhances operational efficiency, standardizes deliverables, and strengthens your competitive edge as a CRO partner.
Every module is built to support accuracy, traceability, and reporting excellence. Continue exploring to learn how Seralogix strengthens compliance, enhances documentation quality, and simplifies preparation for regulatory submissions and audits. Strive for statistically accurate and reproducible study protocols.