A team of passionate scientific writers
In order to convey your study results as effectively and quickly as possible, you need a medical writing team with broad experience in clinical research and local regulatory knowledge. Our medical writers are carefully selected for their competence and passion for the craft of writing. With strong scientific backgrounds from a wide variety of therapeutic areas, and thorough knowledge of GCP and ICH guidelines, our writers are well-equipped to rapidly produce high quality, evidence-backed documents. Once you choose LINK Medical as your strategic CRO partner for medical writing, our priority is to understand your specific needs through active communication in order to deliver our services precisely where you need them. This is a powerful way to free up your team and allow you to focus on other aspects of advancing your product development.
Full life-cycle support
Our medical writing services can support your documentation needs throughout the entire life cycle of your clinical study. Protocol writing in the early stages, as well as clinical study reporting, is supported by our experienced team of biostatisticians and project managers and can be outsourced as part of a full clinical trial package or as a stand-alone service. Once your study is completed, it is important that the results are communicated effectively to a wider scientific audience. To achieve this, our team can provide impactful manuscripts, abstracts, and posters based on your clinical study results.
To find out more about how outsourcing your medical writing can accelerate your product development, contact our Head of Department, Johanna Sundberg.
Overview of Medical Writing services:
- Protocol writing
- Report writing
- Safety narratives
- Patient information sheets
- Development Safety Update Reports
- Updating Investigator’s Brochures
- Communication of study results, e.g. manuscripts
- Register study results in the EudraCT-database
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Clinical Development
