At Stark Pharma, we design, implement, and manage enterprise-grade applications and ERP solutions tailored for pharmaceutical, medical device, and healthcare organizations. Our platforms unify core business functions—R&D, manufacturing, quality, regulatory, finance, and HR—into integrated systems that improve efficiency, enable real-time insights, and ensure regulatory compliance.
We build modular, scalable ERP solutions for life sciences manufacturing and operations. Our flagship StarkERPplatform includes modules for inventory management, production, finance, HR, vendor compliance, and more—optimized for ISO 13485 and FDA 21 CFR Part 11 environments.
We implement enterprise applications that are designed for GxP compliance and validated per CSV and GAMP 5 frameworks. Our approach ensures data integrity, audit readiness, and traceability across all critical business systems.
We help clients select and implement customer relationship management (CRM), supply chain management (SCM), and human resource management systems (HRMS) that align with their operational and compliance needs.
Our team modernizes outdated enterprise systems, ensuring smooth transitions with minimal disruption. We also handle end-to-end data migration and cleansing, preserving integrity and historical traceability.
We automate core workflows such as purchase approvals, batch release, training management, and CAPA tracking. Integrated dashboards provide real-time KPIs and compliance monitoring.
We integrate ERP platforms with third-party tools like QMS, LIMS, eTMF, and regulatory databases to provide a unified digital ecosystem for your life sciences enterprise.
Our systems are purpose-built for the unique needs of pharmaceutical, biotech, and medical device companies—ensuring compliance, scalability, and usability.
We offer ERP solutions that grow with your business. Whether you’re a startup or a multi-site enterprise, our modular architecture supports phased deployments and future upgrades.
With successful deployments across the US, Canada, India, and EU, we bring international regulatory expertise and cross-functional execution capabilities.