Company profile · Skawina, Poland

SyVento BioTech Sp. z o.o.

mRNA Formulation, Lipid Nanoparticle Manufacturing, and Preclinical to Clinical CDMO Services · GMP-capable mRNA and LNP manufacturing

Verified 24 Apr 2026 · 3 sources

CDMOmRNAClinical
PolandCDMOSkawina

Skawina GMP-capable mRNA and LNP CDMO with named CEO, Cytiva FlexFactory platform, and documented preclinical-to-clinical service scope.

Lead
Kajetan Bartosik (verified ↗)
Compliance
GMP-capable mRNA facility
Last reviewed
24 Apr 2026 (2mo ago)
Scale
GMP-capable mRNA and LNP manufacturing
Capabilities
LNP Formulation · mRNA Drug Substance and Drug Product · Preclinical to Clinical CDMO Delivery
Founded
2014
Headcount
1-10
Editorial note

mRNA Formulation, Lipid Nanoparticle Manufacturing, and Preclinical to Clinical CDMO Services

Skawina GMP-capable mRNA and LNP CDMO with named CEO, Cytiva FlexFactory platform, and documented preclinical-to-clinical service scope.

Editorial note

SyVento BioTech anchors Polish mRNA and LNP CDMO capacity with a named CEO, a Cytiva FlexFactory platform, and documented facility opening coverage in Contract Pharma.

FULL TRUST REVIEW COMPLETE
Shown only when all seven trust checks are fully mapped in the directory.
Current review cycleApril 2026Last reviewed: 24 April 2026

Verification details

Site and address
Clinical profileSTATUS: VERIFIED APRIL 2026

Kajetan Bartosik

Chief Executive Officer

Check official leadership source
Full addressul. Za Gora 19, 32-050 Skawina, Poland
Site coordinatesVerification evidence is still being completed.
Review cycle24 April 2026
Physical site source

SyVento registered-office change notice listing Za Gora 19 in Skawina.

Open source
Operating profile

GMP-capable mRNA and LNP manufacturing

Skawina, Poland. mRNA Formulation, Lipid Nanoparticle Manufacturing, and Preclinical to Clinical CDMO Services. Review completed on 24 Apr 2026.

2026 technical specializationmRNA Formulation, Lipid Nanoparticle Manufacturing, and Preclinical to Clinical CDMO Services
Core capabilities
LNP FormulationmRNA Drug Substance and Drug ProductPreclinical to Clinical CDMO Delivery
Governance

Polish Office for Registration of Medicinal Products and EMA for GMP oversight

GMP-capable mRNA facility, Cytiva FlexFactory platform, Contract Pharma facility-opening coverage

Capabilities

LNP Formulation
mRNA Drug Substance and Drug Product
Preclinical to Clinical CDMO Delivery

Sources

The official sources used to verify this profile.

Leadership evidenceSyVento BioTech CEO-appointment announcement naming Kajetan Bartosik as Chief Executive Officer.Source origin: syvento.comOpen source
Supporting evidenceContract Pharma coverage of the SyVento mRNA manufacturing facility opening in Poland.Source origin: contractpharma.comOpen source
Physical-site evidenceSyVento registered-office change notice listing Za Gora 19 in Skawina.Source origin: syvento.comOpen source

Infrastructure

Cytiva FlexFactory platform
LNP formulation workflow
mRNA drug substance and drug product

Certifications

GMP / GLP / ISO-13485 / FDA-Inspected are global quality-system standards. "Verified active" means the directory confirmed the certification is current; "Review in progress" means the cert status is currently being re-verified.

GMP
VERIFIED ACTIVE 2026
GLP
REVIEW IN PROGRESS 2026
ISO-13485
REVIEW IN PROGRESS 2026
FDA-Inspected
REVIEW IN PROGRESS 2026

Review log

24 Apr 2026: Executive identity confirmed via official management disclosure.
24 Apr 2026: Full trust review completed.

Frequently asked questions

Where is SyVento BioTech Sp. z o.o. located?
SyVento BioTech Sp. z o.o. operates from ul. Za Gora 19, 32-050 Skawina, Poland, Skawina, Poland.
Who runs SyVento BioTech Sp. z o.o.?
SyVento BioTech Sp. z o.o. is led by Kajetan Bartosik, Chief Executive Officer. Verified 24 Apr 2026.
What certifications does SyVento BioTech Sp. z o.o. hold?
SyVento BioTech Sp. z o.o. is documented under GMP-capable mRNA facility.
What does SyVento BioTech Sp. z o.o. do?
Skawina GMP-capable mRNA and LNP CDMO with named CEO, Cytiva FlexFactory platform, and documented preclinical-to-clinical service scope. Core capabilities: LNP Formulation, mRNA Drug Substance and Drug Product, Preclinical to Clinical CDMO Delivery.
Editorial context

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