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18 Sept 2025 | Madrid, Spain

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Kseniya Tymko

Business Development Director

Pharmbiotest Poland Ltd

Grudziadz, Poland

1 profile visit

BD Director at CRO Pharmbiotest Poland - a company with over 10 years of experience in Phase I clinical trials, bioanalysis and generic/hybrid drug development.

My organisation

Pharmbiotest Poland Ltd

Pharmbiotest Poland Ltd

Research organization

Grudziadz, Poland

Pharmbiotest Poland is a GLP/GCP-certified CRO specializing in comprehensive clinical research and bioanalytical services. We offer end-to-end clinical trials, covering everything from protocol development to study reporting and secure data/sample storage. Our expertise also extends to the research and development of generic drugs, ensuring high-quality support for pharmaceutical and biotechnological companies. Our Core Services: • Clinical Services – Conducting Phase I studies in our in-house clinical unit, equipped with 38 beds, ensuring high standards of safety and compliance. • Bioanalytical Services – Precise quantification of ultra-low concentrations of small and medium-sized organic molecules in biological samples. Our team specializes in method development, validation, and routine bioanalysis to support clinical trials. • Generic Drug Development – Comprehensive R&D support for the development of high-quality generic medicines, ensuring regulatory compliance and market readiness. We are committed to delivering reliable, high-quality research solutions tailored to the evolving needs of the pharmaceutical industry.
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About me

I’m the Business Development Director at CRO Pharmbiotest Poland — a company with over 10 years of experience in early-phase clinical trials and generic/hybrid drug development. My work is all about building meaningful partnerships with biotech and pharma teams, supporting them at every step — from the first conversation to getting their product into the hands of patients. I believe in clear communication, mutual trust, and solutions tailored to each client's goals. Whether it’s a Phase I trial or a complex bioequivalence study, I’m here to help turn your plans into successful, long-term results.

Social media

Skills

  • Business Development
  • client-focused product development
  • International project management

Interests

  • pharma
  • medtech
  • R&D
  • partnering
  • consulting

Additional questions

Areas od activity

Pharmaceutical industry Laboratory industry Health innovation

Organization type

Research organization

Marketplace (3)

  • Service

    Phase I clinical trials

    End-to-end Phase I trials in one location - from protocol to reporting, with in-house bioanalysis, statistics, and secure archiving.

    • Others
    • Pharmaceutical industry
    Author

    Kseniya Tymko

    Business Development Director at Pharmbiotest Poland Ltd

    Grudziadz, Poland

  • Service

    Bioanalytical Services

    Comprehensive bioanalytical services - from method development to validated LC-MS/MS analysis, reporting, and secure sample storage.

    • Development
    • Laboratory industry
    • Pharmaceutical industry
    Author

    Kseniya Tymko

    Business Development Director at Pharmbiotest Poland Ltd

    Grudziadz, Poland

  • Service

    R&D of Generyc & Hybryd Drugs

    Full-cycle R&D for generic & hybrid drugs — from formulation to trials, bioanalysis, BA/BE/PK, reporting, and CTIS submissions.

    • Consulting
    • Development
    • Health innovation
    • Laboratory industry
    • Pharmaceutical industry
    Author

    Kseniya Tymko

    Business Development Director at Pharmbiotest Poland Ltd

    Grudziadz, Poland