Accelerating Scientific Breakthroughs
Aelius Venture provides compliant, data-driven software solutions that power research, development, and commercialization in the life sciences.
Partner With UsOur Life Sciences Solutions
From the lab bench to clinical trials, we build the digital tools that advance human health.
Building data-centric platforms for drug discovery and research, integrating lab data (LIMS) and bioinformatics analysis.
Developing solutions for electronic data capture (EDC), trial management (CTMS), and patient-reported outcomes (ePRO).
Leveraging AI and machine learning for target identification, molecule design, and predictive modeling in preclinical and clinical phases.
Creating software for genomic data analysis, variant interpretation, and the development of personalized therapies.
Why Aelius Venture for Life Sciences?
In an industry where precision and compliance are non-negotiable, you need a software partner who understands the scientific and regulatory rigors.
Scientific and Regulatory Expertise
We understand the science and the strict regulatory landscape (FDA 21 CFR Part 11, GxP, HIPAA) that governs life sciences software.
Focus on Data Integrity
Our solutions are built to ensure the highest standards of data integrity, security, and traceability, from the lab to the clinic.
Accelerating Time-to-Market
We help life sciences companies accelerate research and development cycles through automation, data integration, and efficient workflow management.
Scalable and Interoperable Systems
We build flexible, scalable platforms that can grow with your research and integrate with other scientific instruments and software.
Proven Success in Life Sciences
See how we've helped biotech and pharma companies innovate faster.
Challenge: A fast-growing biotech company needed a scalable, compliant platform to manage data from multiple global clinical trials, replacing a patchwork of spreadsheets and legacy systems.
Solution: Aelius Venture developed a unified, cloud-based eClinical platform that was fully compliant with 21 CFR Part 11. The system provided modules for EDC, CTMS, and real-time data monitoring, all with robust audit trails.
Outcome: The platform reduced data query rates by 60%, improved data lock times by 50%, and provided clinical operations teams with a real-time, unified view of trial progress, accelerating decision-making.