Side effects and complaints
Due to the new regulatory framework, GDPR (General Data Protection Regulation), we explain below Evolan's way of working
Adverse reaction reports and complaints are handled as follows in accordance with the GVP's Good Pharmacovigilance Practise (GVP) regulations.
Evolan (including all of its legal entities) may store any personal information you share with us. This information will be used to comply with regulatory requirements for pharmacovigilance of medicinal products. The category of personal information that can be archived with initials, birthdays, genderas, dispositives, medical use and living conditions relevant to the adverse event or complaint case and to the use of the drug or product.
The information is electronically stored in a centralized database by Evolan and/or in a paper format on the Evolan archive that senses a limited time. The information can be passed to local bodies and all welcome, and in some cases to other affective pharmaceutical companies, in order to comply with applicable legal requirements. All personal information is handled in accordance with the GVP (Good Pharmacovigilance Practise) and GDPR (General Data Protection Regulation) regulations.
You can request personal information that Evolan stores about you. You have the right to request the rectification of inaccurate personal information about you and to request the removal of the personal information stored. This is done by sending a signed request to Evolan.
Product information and mailings to customers are managed with single download data from the producer Medmind AB. This means that Evolan does not maintain personal data in the form of a customer database. More information about the processing of personal data at Medmind AB can be obtained at www.medmind.se.