I will write a professional icf for clinical trials

Are you looking for a compliant, IRB-ready Informed Consent Form for your clinical trial?

As a PharmD-qualified Senior Medical Writer with hands-on CRO experience at Vivoclin Research Services, I specialize in writing ICFs that meet ICH E6(R2) GCP, FDA 21 CFR Part 50, and EMA standards.

WHY CHOOSE ME?

- PharmD qualified with deep pharmacology knowledge

- Active CRO experience in clinical trial documentation

- 3 clinical trials supported as Clinical Trial Assistant

- Passed 2 regulatory audits with zero critical findings

- PubMed published medical writer

WHAT YOU WILL GET:

- Fully structured ICF with all mandatory sections

- Plain language writing (6th-8th grade readability)

- Therapeutic area-specific content

- Editable Word document with clean formatting

- GCP-compliant, IRB/IEC submission ready

THERAPEUTIC AREAS:

Neurology | Oncology | Psychiatry | Rare Diseases | Medical Devices

WHO I WORK WITH:

CROs | Biotech Startups | Pharma Companies | Independent Researchers | Academic Institutions

Revisions included. Fast turnaround. Regulatory accuracy guaranteed.

Let's get your trial documentation right message me before ordering!