Every clinical study involves medical writing.
Medical writing is more than writing, itās knowing the technical and medical wording and having the language proficiency and skills to illustrate your clinical study through documentation that is clear, accurate, and compliant to supports the planning, execution, and reporting of clinical trials.
easyClinical has medical writers that can rely on producing clinical documents with high quality and efficiency either to support clinical study needs or regulatory and market approvals.
CORE SERVICES
- Protocol & Clinical Investigation Plan (CIP)
- Participant Information Sheet, Consent Form
- Investigator Brochure (IB)
- Operating Manuals
- Clinical Study Report
- Clinical Evaluation Report (CER)
- PMCF Plan
- Abstract & manuscript
- Literature review
SUPPLEMENTARY SERVICES
Capabilities
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Benefits
Our experienced medical writers are specialized in preparing the a spectrum of clinical and regulatory documents needed for clinical trials:
- Protocol, Informed consent form
- Clinical Study Reports (CSRs)
- Investigatorās Brochures (IBs)
- Regulatory submissions (INDs, NDAs, BLAs)
Accurately communicating your study results is crucial to gaining the trust of stakeholders and regulators. Our medical writers help transform complex data into clear, impactful content that supports your clinical objectives:
- Peer-reviewed publications and scientific conference materials
- White papers, conference presentations, and reports
- Consistent documentation across clinical protocols, ensuring accuracy and alignment
Building an in-house medical writing team can be costly and time-consuming. Partnering with easyClinical allows you to:
- Reduce operational costs by accessing specialized expertise without hiring full-time staff.
- Leverage existing templates and processes to streamline document preparation.
- Scale resources up or down based on project needs, ensuring flexibility and efficiency.
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