Basel is the global capital of life sciences, home to Roche, Novartis, and hundreds of biotech companies. The region hosts the world's highest concentration of pharmaceutical expertise. Nulara helps Basel's life sciences companies master complex regulatory requirements and create Digital Product Passports that ensure patient safety.
World Leader in Life Sciences Innovation
The Basel region hosts the world's highest concentration of pharmaceutical and life sciences companies. These organizations face stringent regulatory requirements including FDA, EMA, and Swissmedic compliance. Product traceability, batch documentation, and supply chain transparency are essential for patient safety.
- Headquarters of Roche and Novartis – global pharma leaders
- Over 700 life sciences companies in the region
- World-class research institutions (University of Basel, ETH Basel)
- Tri-national region connecting Switzerland, Germany, and France
Key Industries in Basel
Why Basel Companies Choose Nulara
- Pharma Compliance: Automated documentation for FDA, EMA, and Swissmedic requirements
- Batch Traceability: Complete product genealogy from raw materials to patient
- Clinical Trial Support: Track investigational products through complex trial networks
- Serialization Integration: Connect with existing serialization systems for end-to-end visibility
Enterprise-Grade Security
Frequently Asked Questions
How does Nulara support pharmaceutical regulatory compliance?
Our platform automates documentation for FDA 21 CFR Part 11, EU GMP Annex 11, and other pharmaceutical regulations. We provide audit trails, electronic signatures, and validation documentation that satisfy regulatory inspectors.
Can Nulara integrate with existing pharmaceutical serialization systems?
Yes, we integrate with major serialization platforms including TraceLink, SAP ATTP, and Antares Vision. Our platform aggregates serialization data with other product information to create comprehensive Digital Product Passports.
What batch traceability features does Nulara offer?
Nulara provides complete batch genealogy tracking from raw material receipt through manufacturing, packaging, and distribution. We capture all critical process parameters, deviations, and quality events for each batch.
How does Nulara handle data from clinical trials?
Our platform supports Investigational Medicinal Product (IMP) tracking, blinding requirements, and trial site documentation. We integrate with clinical trial management systems to ensure complete traceability of investigational products.
Ready for DPP Implementation in Basel?
Schedule a personal consultation with our team. We'll show you how Nulara can strengthen your pharmaceutical product data management.
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