How To Write User Friendly Clinical Study Protocol

eBook Download

We are pleased to present you with KomCoord’s first eBook!

Writing a clinical study protocol is an intricate task. The protocol must not only be in compliance with all the applicable laws, regulations, and practices, but it should also be a functional and practical tool for site staff.

What constitutes a “good protocol” may vary for different users. For some, a “good protocol” will be synonymous with an effective study drug or treatment combination. For others, a “good protocol” is a document that is easy to follow, amend or search in.

In the eBook, we share with you our experience, and present 10 ways to create easy-to-read, easy-to-use, easy-to-amend and easy-to-search clinical study protocols. Our aim is to support those who work with protocols, especially those using them at sites on a daily basis.

During the COVID-19 pandemic, when researchers are doing their best to find effective solutions as quickly as possible and the global healthcare system pushes their boundaries to provide the best possible service and care to save lives, a good protocol is more important than ever.

This is the perfect time for those working on protocols to look at them from a different perspective.

We are here to help. We will be happy to review your final document to ensure everything is scripted and laid out to maximize usability and effectiveness.

Download our eBook and get our insights on how to view, write, and design a clinical study protocol to achieve better results.

Download our eBook – How To Write User Friendly Clinical Study Protocol

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