Pharmi assures all aspects of privacy, security & compliance.
How does that work? Read more below.
MedicijnWijs has been developed according to the latest standards in the field of technology safety.
Pharmi BV is ISO 27001 certified and expects to be NEN 7510 certified in 2022.
Two-way authentication, encrypted data transfer, timely updates and security checks protect our users' data.
If you have any questions about security, please contact us.
Pharmi works with the most recent privacy legislation and is supported by the Deloitte Digital Health Compliance group.
Our privacy statement describes the measures we take to protect our user data.
Should you have any questions about privacy, please contact us.
Adequate use of medicines is about the balance between effectiveness and safety.
Safety refers in this context to side effects of drugs.
Pharmi asks users to report experienced side effects. You can report side effects to the doctor or pharmacist, but also via Pharmi.
Gathering side effects makes drug use overall safer.
In case of questions about side effects, please contact us.
Medical devices must comply with new European Medical Device Regulations regulations from 26 May 2021.
MedicijnWijs has been assessed against the current and new regulations regarding medical devices and is not classified as a medical device in its current form.
New products and solutions within Pharmi are always assessed and classified in accordance with the regulations.
Should you have any questions about the medical devices regulations, please contact us.