Clinical research demands rigor. Our platform meets all the regulatory and data security standards required for global trials.
International Conference on Harmonisation Good Clinical Practice guidelines for designing, conducting, recording, and reporting clinical trials.
FDA regulation ensuring electronic records and signatures are trustworthy, reliable, and equivalent to paper records.
U.S. Health Insurance Portability and Accountability Act standards for protecting sensitive patient health information.
European Union General Data Protection Regulation requirements for data privacy and security.
Independent audit confirming our security, availability, and confidentiality controls meet industry standards.
International standard for information security management systems, demonstrating systematic protection of data.
