Scientific Writing

Scientific- Writing-Manuscript-Writing- Pharmaceuticals

  • Clear and concise communication of complex scientific information

  • Expertise in various types of medical and scientific writing, including:

    • Preparation of Briefing Book (BB)

    • Drafting Clinical Study Reports (CSR)

    • Preparation of Investigator’s Brochure (IB)

    • Designing pediatric investigational plans/pediatric study plans (PIP/PSP)

    • Content preparation for CTD Modules (covering 2-5 components)

    • Drafting Toxicology Written Summary

    • Compilation of Non-Clinical Overview

    • Manuscript preparation

  • Our team specializes in crafting compelling manuscripts for publication in prestigious journals such as:

    • Journal of the American Society of Nephrology (JASN)

    • Chemico-biological interactions

    • Pharmaceutical Research

    • Journal of Pharmaceutical Sciences

    • Clinical Pharmacokinetics

    • Infectious Diseases and Therapy

    • Antimicrobial Agents and Chemotherapy (AAC)

    • Journal of Clinical Investigation (JCI)

    • Nature Medicine

    • Translational Research

    • Hepatology

    • Regulatory Toxicology and Pharmacology (RTP), and more

  • Editing and proofreading services for existing documents to improve clarity and readability

  • Experienced with the use of various scientific software and tools to enhance the efficiency and accuracy of writing and data analysis

  • Flexible and responsive to client needs and timelines

Frequently Asked Questions

  • Scientific writing communicates complex data clearly for regulators, researchers, and journals. Professional writing ensures documents are accurate, compliant, well-structured, and impactful, accelerating regulatory approvals and publication success.

  • Yes. SciQra prepares Clinical Study Reports (CSRs), Investigator Brochures (IBs), CTD Module 2–5 content, Toxicology Summaries, and Non-Clinical Overviews. We combine scientific rigor with editorial precision, ensuring compliance with FDA, EMA, ICH, and global regulatory standards.

  • SciQra treats all data with the highest level of confidentiality. SciQra safeguards all data with strict NDAs and secure transfer systems, ensuring sensitive regulatory and clinical information is fully protected.

  • Yes. We offer comprehensive review, editing, gap analysis, and refinement for regulatory and publication documents, ensuring clarity, compliance, and alignment with global standards.

  • Getting started is simple. Contact us through the SciQra website contact page, outlining your project details. Our team will provide a tailored solution, timeline, and delivery strategy, ensuring your documents are scientifically sound and regulatory-ready.