Regulatory & Clinical Writing – Documents & Case Reports
Starting at
$
150
About this service
Summary
I offer writing that supports regulatory submissions, clinical documentation, and case reports that align with industry standards such as ICH, GPP3, and CONSORT. I deliver with accuracy, precision, and scientific integrity from structured protocols to narrative case reports and web-ready clinical articles.
Deliverables
Documents
Includes Clinical Study Reports, investigator Brochures, clinical protocol summaries, and informed consent from.
Case Reports
for journals or internal use
Referencing and Revision
Referencing per ICMJE/AMA style + 1–2 rounds of revisions
What's included
Documents
Includes Clinical Study Reports, investigator Brochures, clinical protocol summaries, and informed consent from.
Case Reports
for journals or internal use
Referencing and Revision
Referencing per ICMJE/AMA style + 1–2 rounds of revisions
Duration
1 week
Skills and tools
Industries
Healthcare