CLINICAL RESEARCH SERVICES - BASED ON YOUR INDIVIDUAL NEEDS

  • DESIGN

    Define and design your clinical outcomes

    Protocol design is key to respond to the scientific questions you are looking to respond to. We can support your team with protocol writing with input from Key Opinion Leaders.

  • STARTUP

    Effective startup to meet your target timelines

    Based on agreed project timelines, we can prepare necessary submissions to obtain approvals from relevant RECs, authorities and biobanks.

  • FEASIBILITY

    Clinical site initiation

    We will support you in identifying the clinical sites where the target patient population is treated, and recruit the ideal clinical sites for your project.

  • STUDY CONDUCT

    Patient recruitment and retention

    Critical to every clinical project, we perform quality assurance at the clinical sites while supporting with recruitment and retention of the defined patient population.

  • DATA COLLECTION

    Effective data collection and cleaning

    Typically the most time-consuming step, we will support the clinical sites to achieve the most effective data collection possible.

  • PUBLICATION

    Making an impact

    Whether we you are looking to publish your data at a congress or a peer-reviewed journal, study reporting will be key to meet your timelines and objectives.

SERVICES

Study feasibility


Protocol writing


REC, CA and biobank applications


Site feasibility


Site initiation


Study reporting


ELEARNING

Elearning course available online - Att planera och genomföra en observationsstudie

Observational research training

Unique course with over 300 study participants

Go from beginner to pro in one day

Self-training designed to make you excel!

Enroll in self-training today!

You get immediate access valid for 14 days.

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