Life Sciences
Accelerating Innovation in Life Sciences Through Digital Transformation
In a rapidly evolving healthcare landscape, Rasta Infotech partners with life sciences organizations to harness the power of digital technologies, accelerate research, streamline operations, and ensure regulatory compliance. From pharmaceuticals and biotechnology to medical devices and clinical research, our tailored digital solutions empower companies to drive scientific breakthroughs, enhance patient outcomes, and bring life-saving therapies to market faster. We enable a digital-first approach across the life sciences value chain — leveraging AI, machine learning, cloud computing, and data analytics to transform drug discovery, clinical trials, manufacturing, and post-market surveillance. Whether you're optimizing R&D pipelines, digitizing regulatory submissions, or ensuring data integrity in GxP environments, our expertise supports innovation with precision and compliance. At Rasta Infotech, we combine life sciences domain knowledge with world-class digital engineering capabilities — our team of bioinformatics engineers, data scientists, cloud architects, and compliance specialists build scalable platforms that deliver clinical, operational, and financial impact across the product lifecycle.
40%
Faster Drug Discovery
60%
Trial Efficiency Gain
100%
GxP Compliance
50%
R&D Cost Reduction
Industry Challenges
Slow Drug Development Cycles
Research and preclinical development hindered by manual processes, siloed data, and the absence of AI-driven molecule modeling and lab automation.
Complex Clinical Data Management
Patient data scattered across systems, manual trial workflows, and difficulty integrating EDC, CTMS, and real-world data sources for unified trial insights.
Regulatory Compliance Complexity
Manual document management, audit trails, and SOP workflows create non-compliance risks with FDA, EMA, and global regulatory bodies.
Data Integrity in GxP Environments
Maintaining ALCOA+ principles — Attributable, Legible, Contemporaneous, Original, Accurate — across digital systems in regulated environments is resource-intensive without automation.
Our Solutions
AI-Powered Drug Discovery Platforms
Develop AI solutions for molecule screening, biomarker identification, and in silico testing to enhance research productivity.
Clinical Trial Digitization
Implement ePRO, eConsent, wearables integration, and remote monitoring tools to optimize patient recruitment and trial outcomes.
GxP-Compliant Application Development
Build and validate enterprise-grade software platforms compliant with FDA 21 CFR Part 11 and global regulatory requirements.
Regulatory Document Management Systems
Create digital platforms to streamline regulatory submissions, automate SOP workflows, and maintain audit-ready documentation.
Real-World Evidence & Analytics
Leverage structured and unstructured datasets to generate actionable insights for market access, pharmacovigilance, and label expansion.
Medical Device Software Engineering
Design and validate embedded and connected software for Class I–III medical devices, ensuring compliance with IEC 62304 and FDA guidance.
Global Pharmaceutical Company
Challenge
Manual clinical trial data management across multiple sites causing delays, compliance risks, and poor real-time visibility into trial outcomes.
Solution
We implemented an integrated EDC and CTMS platform with ePRO, eConsent, wearables integration, and real-time analytics dashboards fully compliant with FDA 21 CFR Part 11 and ALCOA+ standards.
Result
60% improvement in trial data processing speed, full GxP compliance achieved, and 40% reduction in trial operational costs.
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