Batch Certification

SCILO certifies batches of non-sterile medicinal products for human use under manufacturing and importation authorisation no. 260/0612/20, issued by the Chief Pharmaceutical Inspector of Poland. The scope was extended to batch certification and testing of imported medicinal products on 24 June 2026. Sterile products and veterinary medicinal products are outside the scope of our authorisation.

The site holds Certificate of GMP Compliance of a Manufacturer no. WTC/0612_01_01/257, issued on 4 January 2024 following an inspection carried out on 5–6 October 2023. A further inspection was carried out on 2–3 June 2026. The authorisation and the certificate can be verified in the EudraGMDP database.

Transport, customs clearance, storage and distribution remain your responsibility or that of your chosen logistics provider.

Write to info@scilo.eu with the product, the dosage form and the expected number of batches per year.