What specifically do we do for your company?
We know official procedures inside out. We do not write letters that no one reads. We settle matters so that the drug reaches sales without a fight against bureaucracy.
Schedule a 15-minute consultationRegistration of new products
We prepare papers for the Registration Office so that no one has to correct them. We submit applications in the Polish and European systems. Since 2016, we have conducted 142 such processes. We know what errors officials hunt for, so we remove them before you send the documents.
Changes in Permits (Variations)
We handle changes in composition, manufacturing site, or drug name. In 2024, our average time to obtain approval is exactly 34 days. We act quickly so you don't have to suspend deliveries to pharmacies. We watch the deadlines, you handle the sales.
Contact with the Ministry of Health
We represent your interests during talks about drug funding. We know the paths in the MoH departments and funds. Last year, we helped 7 products enter the reimbursement lists. We can also catch errors in penalty calculations – we recovered 1.2 million PLN for one client.
Pharmacovigilance Supervision
We monitor the safety of your products in accordance with the act. We maintain reporting databases and send reports on time. Currently, 23 entities have entrusted us with their drug care. We guarantee constant contact in case of urgent medical signals. No unnecessary paperwork, concretely.
Ready to enter pharmacies?
Don't wait for the office to write to you themselves. Take the initiative and close the process this quarter.
Book a consultation date97.3%
Effectiveness in 2024
Fast track
A preliminary analysis of your case will take us no more than 48 hours.