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Patient Safety and Risk Management

Stragen’s activities as a pharmaceutical company are carried out within a regulated framework at every stage of a drug’s lifecycle, while adhering to latest regulatory requirements and quality standards.

In terms of safety, our medications comply with European regulations. All of our medications are serialized and equipped with a tamper-evident system on each box. Our pharmacovigilance system continously monitor the benefit-risk balance of our medications meeting national and European regulatory requirements.

Certifications and licenses : GDP-certificate and wholesaler licence, Fimea

Pharmacovigilance

For all adverse event suspicion or a security issue concerning our products, please contact Finland’s affiliate:

Or our global pharmacovigilance department

Pharmacovigilance is vital in guarenteeing the safety of medical products. Reportings are essential to ensure a continuous monitoring and in improving the safety of medications. Please feel free to contact Stragen Finland or our pharmacovigilance team if you have any concerns or questions.