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  • ENGLISH
  • FRANCAIS
  • Services
    • Services Overview
    • Clinical Trial Operations
      • Protocol Development and Study Design
      • Feasibility and Study Start Up
      • Patient Recruitment
      • Project Management
      • Clinical Operations
      • Centralized Monitoring
      • Decentralized Clinical Trials (DCT)
      • Centralized eTMF
      • Medical Services
    • Regulatory and Drug Development Consulting
      • Clinical Strategy
      • Nonclinical
      • Chemistry, Manufacturing, and Controls (CMC)
      • Regulatory Affairs
      • GxP Strategy Consulting
      • Publishing and Submissions
      • Medical Writing
    • Government and Public Health Services
    • Biometrics
      • Biostatistics and Statistical Programming
      • Data Management
    • Clinical Pharmacology Modeling Simulation
      • Clinical Pharmacology Integrated Drug Development
      • Model Informed Dose & Drug Development (MIDD)
      • Pharmacometrics (PMx), Pharmacokinetics, Pharmacodynamics (PK/PD)
      • DMPK and Translational Discovery and Development
  • Therapeutic Expertise
    • Therapeutic Expertise Overview
    • By Subject
      • Oncology and Hematology
      • Rare Diseases and Orphan Drugs
      • Infectious Disease and Vaccine
      • Cell and Gene Therapy
      • Central Nervous System
      • Autoimmune and Inflammation
      • Allergy and Asthma
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  1. Home
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  3. Clinical Pharmacology Modeling Simulation
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  5. Scientific/Technical Writing, Manuscripts, and Communication
    • Clinical Study Strategy and Design
    • Development and Regulatory Strategy
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    • Scientific/Technical Writing, Manuscripts, and Communication

Scientific/Technical Writing, Manuscripts, and Communication

  • Clinical Pharmacology Integrated Drug Development
  • Clinical Study Strategy and Design
  • Development and Regulatory Strategy
  • Regulatory Representation, Writing, and Submissions
  • Scientific/Technical Writing, Manuscripts, and Communication

Our focus is delivering high-quality scientific and technical writing, manuscripts, and other communications that are scientifically defensible, well-written, and meet the specifications of target journal(s). Importantly, we also consider how the manuscript or communication will fit into the client’s overall drug development program and messaging.

Allucent takes a team approach to writing that promotes scientific rigor, clear messaging, and efficiency by working closely with our clients to understand not only the nuances of a particular study but also the messages that the client wishes to convey. Our approach is unique because our team has a deep understanding of clinical pharmacology and the impact of what they’re writing.

In addition to scientific/technical and manuscript writing, we also offer review services that provide the same expert review for our client’s manuscripts as for manuscripts we have written ourselves. We can also assist in formatting, strategies for addressing reviewer comments, or even suggestions for an appropriate target journal. Allucent’s scientific/technical and medical writing teams are positioned to deliver high-impact external data dissemination for abstracts, posters, manuscripts, presentations, AdBoard preparation, and/or press releases as needed.

Technical Writing and Manuscript Services:

  • Abstracts (Posters and Presentations)
  • Full Manuscript Authoring
  • Ghost Authoring
  • Literature Searches
  • Scientific Review
  • Review for Writing Conventions and Journal Standards
  • Target Journal Recommendations
  • Manuscript Revisions
  • Advisory Board presentations
  • Press releases

Contact Us

Let us partner with your team on bringing new therapies to light. Get in touch to get started.

CONTACT US

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