Cloud Built for Pharmaceuticals
Accelerate drug discovery, manage clinical trials, and maintain regulatory compliance with GxP-validated cloud infrastructure designed for the pharmaceutical industry's most demanding workloads.
Compliance & Certifications
Accelerate the drug discovery pipeline with high-performance computing for molecular dynamics simulations, virtual screening, and AI-driven compound optimization. MassiveGRID provides the GPU clusters and storage infrastructure required for computational chemistry at scale.
Molecular Dynamics
GPU-accelerated molecular dynamics simulations using GROMACS, AMBER, and NAMD. Model protein folding, drug-receptor interactions, and binding affinity calculations on dedicated HPC clusters.
AI Drug Design
Train deep learning models for de novo molecule generation, ADMET property prediction, and lead optimization. GPU clusters support transformer models and graph neural networks for computational drug design.
Genomics & Bioinformatics
High-throughput sequencing data processing pipelines for whole genome sequencing, RNA-seq, and proteomics. Scalable storage for petabyte-scale biobank data with fast parallel I/O for bioinformatics workflows.
Virtual Screening
Screen billions of compounds against target proteins using molecular docking and pharmacophore modeling. Distributed computing across hundreds of nodes accelerates hit identification from months to days.
Manage global clinical trials with infrastructure validated for 21 CFR Part 11 compliance. From electronic data capture to randomization systems and safety databases, MassiveGRID supports the full clinical trial lifecycle with validated, auditable infrastructure.
Electronic Data Capture (EDC)
High-availability hosting for EDC systems with 21 CFR Part 11 electronic signature support, complete audit trails, and role-based access control. Support multi-site trials across dozens of countries simultaneously.
Randomization & Trial Supply
Interactive response technology (IRT) infrastructure for patient randomization, drug supply management, and dosing algorithms. Real-time inventory tracking ensures trial continuity across global investigator sites.
Safety & Pharmacovigilance
Safety database hosting for adverse event reporting, signal detection, and regulatory submissions. Automated MedDRA coding, CIOMS form generation, and expedited reporting to health authorities worldwide.
Clinical Analytics & Biostatistics
High-performance computing for SAS, R, and Python-based statistical analyses. Support adaptive trial designs, interim analyses, and submission-ready statistical outputs with validated computing environments.
Maintain continuous compliance with FDA, EMA, and global regulatory requirements. MassiveGRID provides validated infrastructure for manufacturing execution systems, quality management, and electronic regulatory submissions with complete documentation packages.
Manufacturing Execution (MES)
GMP-validated hosting for manufacturing execution systems. Batch record management, equipment integration, environmental monitoring, and real-time production analytics for pharmaceutical manufacturing facilities.
eCTD Submissions
Infrastructure for assembling and publishing electronic Common Technical Document (eCTD) regulatory submissions to FDA, EMA, PMDA, and other health authorities. Document management with lifecycle tracking and version control.
Quality Management (QMS)
Validated hosting for quality management systems including CAPA, deviation management, change control, and document control. Integrated audit management with regulatory inspection readiness.
Why 100% Uptime Matters for Pharma
Drug discovery timelines, clinical trial data integrity, and regulatory submissions all depend on infrastructure that never goes down.
Platform Features
Infrastructure engineered for pharmaceutical workloads
GxP Validated
Infrastructure qualified per GAMP 5 with IQ/OQ/PQ documentation and ongoing validation maintenance.
GPU Clusters
NVIDIA GPU clusters for molecular dynamics, AI drug design, and genomics processing at scale.
21 CFR Part 11
Electronic signatures, audit trails, and access controls meeting FDA 21 CFR Part 11 requirements.
Petabyte Storage
Scalable object storage for genomics data, imaging archives, and clinical trial datasets.
Global Compliance
Data residency options for FDA, EMA, PMDA, and other regulatory jurisdiction requirements.
Pharma Support
Dedicated support engineers with pharmaceutical IT expertise available 24/7.
500+ Datacenters Worldwide
Deploy on Equinix and Digital Realty infrastructure across 6 continents.
Americas
US, Canada, Brazil, Mexico
Europe
UK, Germany, France, Netherlands
Asia-Pacific
Singapore, Tokyo, Sydney, Hong Kong
MEA
Dubai, South Africa, Kenya
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Ready to Accelerate Your Drug Pipeline?
Talk to our pharmaceutical cloud specialists about GxP-validated infrastructure for drug discovery, clinical trials, and manufacturing.