Call Us: +48 668 221 763

  • Batch certification and quality control testing of medicinal products

    SCILO holds a manufacturing and importation authorisation issued by the Chief Pharmaceutical Inspector of Poland. Our Qualified Person certifies batches of non-sterile human medicinal products. Testing and certification are done at one site.

  • A GMP laboratory near Łódź

    Chemical and physical testing of medicinal products, starting materials and finished products, method development, transfer and validation, stability studies.

SCILO sp. z o.o. is a pharmaceutical laboratory operating under GMP in Prusinowice, Poland. We test medicinal products, starting materials and finished products, and we certify batches before they are released to the market.

Manufacturing and importation authorisation no. 260/0612/20 was issued by the Chief Pharmaceutical Inspector on 14 December 2020. On 24 June 2026 its scope was extended to batch certification of non-sterile medicinal products for human use.

GMP compliance of the site was confirmed by 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. Both the authorisation and the certificate can be verified in the EudraGMDP database.

Batch certification

Our Qualified Person certifies batches of non-sterile medicinal products for human use. Testing and certification are done at one site, by the people who ran the analysis.

Quality control testing

Chemical and physical testing of medicinal products, starting materials and finished products, using pharmacopoeial methods or methods transferred from your site. HPLC, gas chromatography including headspace and direct injection, dissolution testing, and particle size determination by air-jet sieving.

Analytical standards

Primary standards, EP primary standards, API working standards and impurity standards. We source hard to find standards and support custom synthesis on request.

GMP and GDP Auditing

Audits of manufacturers of medicinal products, producers and distributors of API, producers of packaging materials and excipients, laboratories, transport companies and pharmaceutical wholesalers.

Consulting and training

Establishing and maintaining quality management systems, with a focus on quality control laboratories. Training on validation, transfer and verification of analytical methods, HPLC and UPLC troubleshooting, GMP, GDP and supplier auditing.

Where our scope ends.

Our authorisation covers testing and batch certification. Transport, customs clearance, storage and distribution stay on your side or with your logistics provider.

Write to info@scilo.eu or call +48 668 221 763. Tell us the product, the dosage form, the methods you use and the number of batches, and you will get a quotation with a price and a date.

A FEW OF OUR VALUED CLIENTSall of them are satisfied

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