DEVELOPMENT & MANUFACTURING COLLABORATION

Continue the conversation with Stasinos Chr. Sikalias

Let’s discuss manufacturing, development, European nearshoring and raw materials for your next project.

The Sikalias building at 7 Kyklaminon Street, Peristeri

INDUSTRIAL COLLABORATION · ATHENS, GREECE

A clear starting point for your project

CMO · Transfer & manufacturing

Bring your dossier, dosage form and forecast for a technology-transfer and manufacturing assessment.

Discuss CMO

CDMO · Development & dossier strategy

Discuss commissioned development or a dossier in preparation, with scope, rights and future manufacturing agreed for the project.

Discuss CDMO

European nearshoring

For complex-molecule projects and biotechnology startups seeking a European development or manufacturing partner. Technical fit, analytical needs and the authorised scope are assessed first.

Discuss your nearshoring project

R&D raw materials

Introduce an exact API, excipient, extract or functional ingredient grade for an assigned R&D project.

Introduce your materials

Quality documents

Request the current site-specific qualification package from the Laboratories’ QA team.

Request quality documents

Start with a non-confidential outline: product category, dosage form, target market, development stage and expected scale. The next step is a technical fit assessment; a public description is not a commitment to manufacture every technology.

From an introduction to a working project

Initial fit → confidentiality agreement where needed → technical and regulatory feasibility → agreed scope and quotation → development or transfer → manufacturing. The project enquiry is the starting point for a technical discussion with the appropriate team.

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Stasinos Chr. Sikalias · Pharmacist, Managing Director & R&D Manager

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Manufacturing partner

Explore the Laboratories’ project pathways and technical platform.

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Scientific background

Read selected scientific notes and presentations.

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A focused next step

Send a non-confidential outline of your product, dosage form, development stage, target market and expected scale. The next step is an assessment of the technical and authorisation fit.