KLIFO can offer you a wide range of services related to clinical trials and clinical investigations. Our services are personalised to your specific needs. We have experience in phase I to IV trials and work across the world. As a partner member of PSN, we have an extensive geographical operational reach.

Our team consists of experienced Project Managers (PM), Clinical Research Associates (CRA) and Clinical Trial Administrators (CTA) with experience in the industry and with CROs.

A focus on quality

Because we have a fully implemented quality system, our services comply with EU and local requirements.

Clinical Trial Services is regularly audited by our clients. Our Clinical QA Manager is responsible for managing quality assurance activities within Clinical Trial Services, and for ensuring compliance with international and national regulations and guidelines.


Areas of expertise

We offer in-depth knowledge of clinical development and the management of all aspects of clinical research, including feasibility and site selection, protocol preparation, application to authorities and ethics committees, project management, monitoring, pharmacovigilance and medical writing.

KLIFO has experience in working with a range of different clinical trials, including:

  • Phase I to IV trials
  • First-in human (FIH) trials
  • Clinical investigations
  • Trials in Scandinavia
  • International trials in Europe and the U.S. under the auspices of PSN.

Our services

KLIFO offers in-depth knowledge of clinical development and management of all aspects of clinical research, including feasibility and site selection, protocol preparation, application to authorities and ethics committees, project management, monitoring, pharmacovigilance and medical writing.

Examples of our services include:

Trial management

  • Clinical trial synopsis
  • Clinical trial protocol
  • Site feasibility and site selection
  • Submission of clinical trial application to authorities and ethics committees
  • Initiation of clinical sites
  • Interim monitoring of clinical sites
  • Closing of clinical sites
  • Clinical study reports
  • Clinical project management
  • Pharmacovigilance.

Data management and statistics

  • eCRFs and CRFs
  • Through our partnership with BioStata (www.biostata.com), we provide data management and statistical services
  • Statistics.

Medical device

  • Clinical investigational plans
  • Submission to authorities and ethics committees
  • Monitoring
  • Clinical investigational reports.

Geographical coverage

KLIFO Clinical Trial Services has its own operational staff and covers Scandinavia.

KLIFO is part of the international CRO PSN Research, which enables us to conduct international clinical studies with own staff in most of Europe and the U.S. We regularly lead or participate in international clinical trials and investigations covering Scandinavian countries.

  • Lisbet Vandvig

    Lisbet Vandvig
    MD

    Vice President, Clinical Trial Services & Pharmacovigilance Services

    T: +45 44 222 921
    E:

KLIFO is a partner in PSN, an international full-service CRO with operational activities across Europe and North America.

Since 2011, KLIFO has worked in partnership with BioStata ApS regarding Data Management and Statistics.

BioStata has more than 20 years of experience in Data Management and Statistics. KLIFO and BioStata have successfully worked together as one team on several projects.