CLINBIT


Provider of clinical trial support services in the European Union, offering feasibility assessments, study start-up, regulatory submissions, patient recruitment, clinical monitoring, project management and GCP training. Operates with multi-decade experience and supports a range of therapeutic areas.

Industries

biotechnology
clinical-trials
electronic-health-record-ehr
project-management-db17

Nr. of Employees

small (1-50)

CLINBIT

Kraków, Malopolskie, Poland, Europe


Services

Assessment of country- and site-level feasibility and enrollment projections to inform site selection and milestone planning.

Document preparation and review, contract and budget negotiations, and site activation support.

Preparation of regulatory submissions, adaptation of patient materials to local requirements and liaison with regulatory authorities.

Creation and execution of enrollment plans, recruitment materials, and coordination with patient associations and site networks.

Monitoring visits and oversight to ensure protocol adherence, data integrity and regulatory compliance.

Full project management for clinical trials including timeline, budget and team coordination across therapeutic areas and phases.

View All Services

Expertise Areas

  • Clinical trial management
  • Site feasibility and activation in EU countries
  • Regulatory submissions and local compliance (EU)
  • Participant recruitment and enrollment strategies
  • Show More (3)

News & Updates

Company reports over 20 years of involvement in clinical research.

Company reports conduction of 25 clinical trials.

Company lists core therapeutic areas including cardiology, pediatrics, gastroenterology, pulmonology, oncology and hematology.


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