Contract manufacturing

Looking for a partner who can guarantee high-quality pharmaceutical manufacturing compliant with international standards? We offer flexible collaboration models – from product and formulation development, through technology transfer, to full-scale manufacturing of finished medicinal products. Our state-of-the-art facilities are designed to produce a wide portfolio of forms and doses – including highly potent medicines (up to OEB 5) – ensuring full process integrity and operator safety.

We manufacture over 25 million packages annually, handling both small batches and large-scale volumes. The integration of R&D, quality control, and production enables us to efficiently scale up projects to industrial production. We focus on a partnership-based approach that ensures predictability, efficiency, and full compliance with EU cGMP, FDA, and EAEU requirements.

Learn more about our contract manufacturing capabilities.

Possible cooperation models

CDMO
CMO
Licence-In
Licence-Out

Produced pharmaceutical forms

Tablets and capsules

Powders for suspension

Lyophilisates for injectable solutions

Injectable solutions and suspensions

Gels and pharmaceutical aerosols

Tablets and capsules

Powders for suspension

Lyophilisates for injectable solutions

Injectable solutions and suspensions

Gels and pharmaceutical aerosols

Tablets and capsules

Powders for suspension

Lyophilisates for injectable solutions

Injectable solutions and suspensions

Gels and pharmaceutical aerosols

Tablets and capsules

Powders for suspension

Lyophilisates for injectable solutions

Injectable solutions and suspensions

Gels and pharmaceutical aerosols

Why partner with us?

200 YEARS OF EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY

Over two centuries of experience have enabled us to develop a comprehensive pharmaceutical offering that continues to evolve in response to the changing needs of patients and business partners.

CAPACITY TO MANUFACTURE HIGHLY POTENT MEDICINES

We manage projects involving high-potency compounds up to OEB 5 on state-of-the-art production lines, ensuring full process safety and compliance with cGMP (EU), FDA and EAEU requirements.

FULL PROCESS INTEGRATION UNDER ONE ROOF

We combine research, development, Quality Control (QC) and industrial-scale production to ensure fast, reliable and scalable project delivery while maintaining full process oversight.

COMPREHENSIVE PORTFOLIO OF DOSAGE FORMS

We specialise in the production of active pharmaceutical ingredients (APIs) and finished dosage forms (FDFs). Our facilities produce over 50 products in more than 130 forms and doses – from tablets and capsules, through sterile injections and lyophilisates, to aerosols and gels.

FLEXIBLE COOPERATION MODELS

We tailor our partnership models to individual project needs – CDMO, CMO, Licence-In & Licence-Out – ensuring flexibility at every stage of collaboration.

VARIOUS THERAPEUTIC CLASSES

We specialise in antibiotics, human insulins, dermatological and central nervous system (CNS) medicines, offering expert knowledge and experience across each therapeutic area.

Need more information?

Contact us to discuss your project and see how our CDMO/CMO expertise can be tailored to your product’s needs.

Our specialists will be pleased to explore cooperation opportunities
and prepare a detailed proposal.

cmo@tzf.pl