Food Industry & Nutrition
Clinical trial software for food industry and nutrition studies
oomnia brings together EDC, CTMS, eTMF, RTSM, and participant‑focused solutions within a single Clinical Research Information System (CRIS), helping food and nutrition teams manage diverse data and complex study workflows in one place
Industry Challenges
Industry challenges in food industry and nutrition studies
Running food and nutrition studies comes with distinct operational complexity due to real‑world conditions and human variability. Key challenges include:
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Differences in diet, habits, and participant compliance impacting consistency
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Strong reliance on self‑reported intake and subjective outcomes
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Difficulty aligning endpoints across nutritional, functional, and behavioral metrics
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Disconnected data sources including apps, wearables, labs, and surveys
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Limited ability to track long‑term nutritional impact reliably
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Coordination challenges between in‑clinic, at‑home, and digital environments
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Data gaps caused by fragmented systems and inconsistent reporting
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Lack of immediate visibility into adherence and study progress
Our Solution
Wemedoo's clinical trial solution for food industry studies
oomnia delivers a unified environment tailored for nutrition and food research programs:
Single platform for study operations
All functionalities operate within one integrated CRIS framework
Centralized view of study data
Continuous access to dietary intake, participant activity, and outcomes
Consistent execution across studies
Standardized processes across intervention and observational study designs
Integrated data ecosystem
Combines clinical, dietary, and digital inputs into one structured dataset
Adaptable study setup
Flexible configuration supports protocol adjustments without disruption
The Platform
Clinical trial capabilities across food and nutrition studies
eConsent software
Digital consent workflows for compliant and remote enrollment
EPROePRO software
Ongoing capture of dietary intake and participant feedback
RTSMRTSM software
Allocation and supply workflows for controlled nutrition trials
CTMSCTMS software
Operational management across sites and study phases
EDCEDC software
Unified data capture from clinical and dietary sources
ETMFeTMF software
Organized trial documentation with full accessibility
ECOAeCOA software
Digital clinical outcome assessments across stakeholders
ESOURCEeSource clinical trials
Direct data entry at source, minimizing manual duplication
Why It Matters
Why unified clinical trial software matters for food industry studies
Food and nutrition research often depends on multiple disconnected tools for tracking diets, outcomes, lab results, and engagement. This separation creates inefficiencies and weakens data reliability.
A centralized Clinical Research Information System (CRIS) consolidates all study components into a single environment, allowing smoother data exchange, stronger oversight, and more efficient study execution.
Modular eClinical Systems
Split across multiple tools and vendors
Variability from multiple data sources
Manual merging of datasets
Slower due to fragmented workflows
Unified Clinical Trial Software (oomnia)
Seamless real-time flow within one platform
Harmonized data structures across studies
Minimal reconciliation due to shared data model
Faster execution across processes
SIDE BY SIDE
Modular eClinical system vs. Unified clinical trial software
| Area | Modular eClinical systems | Unified clinical trial software (oomnia) |
|---|---|---|
| Data flow | Split across multiple tools and vendors | Seamless real‑time flow within one platform |
| Data consistency | Variability from multiple data sources | Harmonized data structures across studies |
| Reconciliation | Manual merging of datasets | Minimal reconciliation due to shared data model |
| Risk of errors | Higher due to inconsistencies | Lower with structured, unified data |
| Monitoring | Limited tracking of adherence | Continuous real‑time monitoring |
| Team workload | Time spent consolidating data | Focus shifts to insights and decision‑making |
| Data quality | Increased risk of gaps or inconsistencies | Improved through validation and structure |
| Operational speed | Slower due to fragmented workflows | Faster execution across processes |
| Scalability | Difficult to expand programs | Supports growth across regions and studies |
Regulatory Readiness
Compliance and regulatory readiness
oomnia supports compliance requirements relevant to food and nutrition research while ensuring transparency and data integrity:
21 CFR Part 11
Compliance with 21 CFR Part 11
ICH E6(R3) alignment
Alignment with ICH E6(R3) principles where applicable
CDISC-compatible formats
CDISC‑compatible data formats for reporting
GDPR data protection
GDPR‑aligned data protection and privacy handling
Audit logs and traceability
Complete audit logs and traceability
Validation support
Ongoing validation support for regulated environments
Get Started
Scale food and nutrition studies with full visibility
Discover how a unified platform can help manage complex nutrition studies, enhance data consistency, and provide continuous oversight across participants and sites.
Talk to our team