CLINICAL RESEARCH SERVICES - BASED ON YOUR INDIVIDUAL NEEDS
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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.
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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.
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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.
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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.
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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.
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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.
