Pharmaceuticals
GxP-compliant research infrastructure, clinical trial data management, and regulatory submission systems built for pharma on AWS.
Pharmaceutical companies operate under some of the most rigorous regulatory requirements in the world, managing complex clinical trial data, GxP-compliant manufacturing systems, and global regulatory submission processes. Cloud Life Consulting builds AWS infrastructure that meets FDA, EMA, and international pharmaceutical regulatory requirements.
By the numbers
21 CFR
Part 11 and GxP compliant infrastructure for pharmaceutical data management and clinical systems on AWS
50%
Reduction in research compute costs after migrating clinical trial data processing to AWS Spot and Graviton
99.99%
Uptime achievable for clinical trial management and regulatory submission systems on AWS multi-AZ architecture
What we build for you
21 CFR Part 11 and GxP compliant data management with electronic records, audit trails, and e-signatures
Clinical trial data platforms with CDISC-compliant data management and regulatory submission readiness on AWS
High-performance research computing using AWS Batch and Graviton for genomics and computational chemistry
Manufacturing execution system integrations with GMP compliance monitoring and batch record management
Generative AI on AWS
Cloud Life helps pharmaceutical companies deploy Amazon Bedrock and SageMaker for drug candidate analysis, clinical outcome prediction, and automated regulatory document drafting.
Cloud Life builds GxP-compliant AWS infrastructure for pharmaceutical organizations managing clinical data, regulatory submissions, and research computing at scale.
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