Life Sciences & MedTech
Balancing innovation velocity with GMP compliance and data integrity. We help leaders modernize manufacturing without compromising on quality.
In Life Sciences, the cost of error is existential. Yet, the pressure to reduce time-to-market for therapeutics and devices has never been higher. AT LOCHS RIGEL, we provide the engineering depth and regulatory intelligence required to navigate this tension.
Strategic Priorities
Paper-to-Glass Transition
Digitizing batch records (eBR) and quality management systems to reduce manual error, increase data integrity, and minimize audit risk.
Serialization & Traceability
Implementing robust, secure track-and-trace systems to meet evolving global regulatory requirements while improving supply chain visibility.
Lab-to-Fab Scaling
Accelerating technology transfer from R&D to commercial manufacturing through modular automation and scale-up engineering.
Validated Cloud Architectures
Designing GxP-compliant cloud and edge infrastructure that enables real-time analytics while maintaining strict validation standards.
Compliance-Ready Engineering
Our teams include Computer System Validation (CSV) experts who ensure every digital and automation initiative is audit-ready and production-stable from day one.
Secure Your Pipeline
Discuss your GMP modernization strategy with our subject matter experts.
Audit-Ready Logic // Technical Depth