Our medical writers help you in the preparation of the following:
Clinical study protocols
Informed consent forms
Study assessment questionnaires
Clinical study reports – Phase I to IV
Abstracts and manuscripts
Clinical overview and Clinical Summary
Our medical writing services are based on our extensive experience in the pharmaceutical industry and our commitment to quality, which ensures clear, concise and well-structured documents.
Croissance Clinical Research has a team of experienced medical writers with medical and scientific expertise to provide high quality clinical study documents compliant with ICH-GCP guidelines and regulatory requirements.
From protocol writing to the final study report preparation, our medical writers collaborate with bio-statisticians and project team members to produce comprehensive, submission-ready documents for all stages of clinical development.
All documents are peer reviewed to ensure medical and scientific accuracy and are subjected to continuous quality control to guarantee compliance ensuring high quality deliverable, on-time. We provide medical writing services as part of the comprehensive clinical trial program or as a stand-alone service.
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