Promente Clinical Research Center

For CROs and sponsors

Partner with an experienced clinical research site in Bydgoszcz, Poland.

Clinical research team members review study documentation with a CRO partner.

Why work with Promente?

Experienced team

Investigators, raters and coordinators who have worked together for years.

GCP awareness

Good Clinical Practice is treated as a practical standard across the team.

Patient safety

The principal investigator and sub-investigators actively supervise participant safety and protocol adherence.

Participant comfort

The site pays attention to participant and caregiver comfort during visits.

Vendor cooperation

The site works with specialist vendors and supports operational continuity.

Team backup

Backup is planned for key team roles to protect continuity of study work.

Site infrastructure

  • Basic and specialist research equipment with valid certificates.
  • Secure investigational product access and storage procedures.
  • Air-conditioned and mechanically ventilated rooms.
  • Specialist refrigerators and freezers for biological materials and investigational products.

Discuss site cooperation

Contact us to discuss a clinical trial feasibility or collaboration.