In collaboration with our clients in life sciences, Novo Compliance’s virtual and embedded resources assist our clients interpret, develop and operationalize evolving health authority requirements associated with global Digital Health Technologies (DHTs), ensuring compliance across pre-clinical and clinical trials, collecting, analyzing and inculcating real-world data, real-world evidence, post-market commitments. and surveillance. Our bespoke Regulatory Strategic ARC® assisting our clients assess global regulations, standards and guidance’s, from health authorities global remote monitoring frameworks to digital endpoints, translating into actionable strategies that align with health authorities’ regulatory expectations. By harmonizing technical validation, data integrity, and patient-centric design, Novo Compliance empowers our clients and life sciences organizations, developing, deploying and maintaining DHTs confidently while accelerating innovation and regulatory readiness.