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Planning your research

Getting your study design correct from the very beginning is the best way to make sure your great idea leads to solid and reproducible results. Our consultants are experienced in setting up clinical, in vivo, and in vitro studies of pharmaceuticals, biomarkers, and medical devices. Contact us to discover how we can help you build a solid foundation for your upcoming research project.

We can help you with:​​

Scientific advice: Our consultants help you incorporate good research practices into your study plan, taking into account the applicable guidelines and checklists for your specific type of study.​

Medical writing: A lack of time or resources shouldn't keep you from creating a robust and reliable research plan. Our consulting team includes expert medical writers who can step in and write documents relating to your research plan, including:

Grant applications:

  • Innovation grants (Vinnova, SSF, etc.)

  • Academic grants (VR, ALF, etc.)

  • International grants

Regulatory documents:

  • Clinical evaluation

  • Orphan drug designation application

  • Investigator's brochure

Study protocols:

  • Clinical trial protocols

  • Registered reports

  • Systematic review protocols

  • Statistical analysis plan​s


Standard operating procedures:

  • Sample collection and biobanking

  • Assay validation

  • Data analysis

Language editing: Our native English-speaking medical writers and editors help polish your writing to make sure your ideas are presented clearly and concisely.

And more... Contact us for more information.

Do you already have a great plan in place? Learn how we can help you run your project.

Done with your project and ready for the next step? Learn how we can help you report your results.

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