To enhance our website and services, we use Google Analytics, which requires your consent below to gather data about your device and site usage. Your data may be transferred outside the EU by Google, where regulations may differ. Consent is voluntary and revocable by contacting us.
Essential cookies are strictly necessary for site operation. For details on cookie usage as well as how we process your data, please read our policy.
Designed with the healthcare industry in mind, the US FDA 21 CFR Part 11 regulations outline criteria for accepting electronic records and electronic signatures as equivalent to paper-based records and handwritten signatures. FDA 21 CFR Part 11 also provides guidelines for documenting and validating authorized change processes to systems and software involved in the creation of electronic documents.