Pharmaceutical and life sciences organisations require infrastructure that is GxP-compliant, sovereign, and capable of handling the most data-intensive compute workloads in science — from drug discovery AI to clinical trial data management.
What the industry faces.
GxP & Regulatory Compliance
FDA 21 CFR Part 11, EU Annex 11, and CDSCO requirements demand validated, auditable infrastructure with complete data integrity.
Drug Discovery AI
Molecular dynamics simulation, protein folding, and generative chemistry AI require massive GPU compute clusters on-premise.
Clinical Trial Data Security
Patient-identifiable clinical trial data must remain within national boundaries with complete audit trails and access controls.
Manufacturing Compliance
Pharma manufacturing systems require hardened infrastructure for SCADA, batch record management, and quality control.
Multi-Site Research Collaboration
Distributed research teams need infrastructure that enables secure collaboration across sites without data sovereignty compromise.
Long-Term Data Retention
Regulatory requirements mandate 25+ year data retention for clinical trial records and drug approval documentation.
Built for your needs.
Planck sovereign edge data centers provide GxP-validated, compliant infrastructure for pharmaceutical research and manufacturing — from GPU-dense drug discovery compute to compliant clinical data platforms.
Recommended for this industry.
Q10
High-performance edge infrastructure for GPU-dense drug discovery and research AI workloads.
Learn moreSovereign Cloud
Clinical data sovereignty with national control and GxP-aligned compliance frameworks.
Learn moreEdge AI Fabric
Distributed AI infrastructure for drug discovery, clinical analysis, and research AI.
Learn moreAI Data Lakes
Compliant research data management with long-term retention and high-performance access.
Learn moreLet's build your edge infrastructure.
Talk to our team about your specific requirements and deployment timeline.