COMPANY OVERVIEW · SEPTEMBER 2026

From formulation challenge to manufacturing programme.

Sikalias Pharmaceutical Laboratories SA · Two complementary manufacturing sites in Peristeri, Athens.

Four routes to collaboration

CMO

Technology transfer and manufacturing from the client’s dossier.

CDMO

Development, technical documentation and subsequent manufacturing, with an agreed regulatory pathway.

R&D materials

Project-based evaluation of APIs, excipients, extracts and functional ingredients.

Nearshoring

A European base for complex-molecule and biotech startup programmes: drug-product development, transfer and non-sterile manufacturing assessment.

Explore the approach →

Technical platform

Non-sterile oral liquids, topical and semisolid products, sprays and drops, hard capsules, tablets and powders. Low-humidity room below 10% RH, nitrogen capability on selected liquid lines, and integrated production and packaging flows.

Quality & qualification

Project-specific site selection, authorisation scope, technical transfer, stability and validation planning. QA provides the controlled quality package. Site 1 now also has GMP certification; QA provides the current site-specific certificate, authorisations and exact scope for project qualification.

Quality documentation

Continue the conversation

info@sikalias.com · +30 210 572 0900 · https://sikalias.com/partners/

Site 0: 7 Kyklaminon str., Ag.Ierotheos, Peristeri, 12137, Greece
Site 1: 3–5 Stilianou Gonata str., Peristeri Industrial Park, 12133, Greece