Medisafe ISO 27001:2013 Certificate

Medisafe Certification for Medical Platform Security Management

ISO 27001-2013Medisafe is ISO 27001:2013 certified, meeting all IT security management system standards specific to medication and digital health platforms.

What’s the ISO?
The International Organization for Standardization (ISO) is an independent, non-governmental organization with a membership of 167 national standards bodies. It is based in Switzerland and develops voluntary, consensus-based, market relevant worldwide that support innovation and provide solutions to global challenges.

What’s “ISO 27001:2013 certified” mean?
This certification specifically sets out quality assurance standards that sensitive information such as user data, logins, network traffic, storage and backups are managed in a secure manner. This means Medisafe’s security has been independently audited and shown to be operating to the highest international standards for medical platforms.

How does this help Medisafers?
We are committed to your privacy and this certification ensures that sensitive information is handles at the highest international security standards for medical platforms. The ISO 27001:2013 standard is voluntary and the standards for certification are high. For example, Medisafe is required to produce intensive documentation, detailed risk assessments, proof of internal training, audits and other documentation on a regular basis, with annual accreditations and reviews by an independent third party.

Because ISO 27001 certification is so demanding, few companies actually undertake the certification process: Only 40,000 of the 335 million companies worldwide are ISO 27001:2013 certified.

Download our ISO 27001: 2013 Certificate

You may also like

PDURS: 7 Experts to Follow As the Draft FDA Guidelines Progress

Want to keep current on the FDA’s Draft Guidelines for Prescription Drug Use Related Software (PDURS)? Follow the LinkedIn profiles 

..Read More

PDURS: What Four Top Law Firms Are Saying

The FDA’s draft guidelines for Prescription Drug Use Related Software (PDURS) have drawn significant attention from the legal community. Law 

..Read More

PDURS: How 7 Companies and Groups Responded to the Draft Guidelines

The FDA’s Draft Guidelines for Prescription Drug Use Related Software (PDURS) have sparked considerable discussion among various stakeholders, including pharmaceutical 

..Read More

Want to Learn More?

We bring decades of experience to your challenges—and technology and solutions uniquely designed to meet your needs.