Our Services
We’re committed to delivering high-quality content that’s tailored to your needs.
Our specialized regulatory and publications medical writing services support teams working in oncology and immunology. We collaborate with a wide range of clients in industry and academia to offer flexible assistance at all stages of drug development.
Medical
Writing
End-to-end oversight to uphold deadlines, improve communication, and align stakeholders across teams.
Project
Management
Communicating complex science with clarity and precision through high-quality documents.
Strategic Consulting
Targeted guidance on study design, regulatory strategy, and document planning to meet agency expectations.
Deliverables
Our deliverables reflect a commitment to precision, compliance, and clarity, ensuring each document not only meets regulatory expectations, but also advances the collective mission of bringing innovative therapies to patients.
Regulatory Writing
Investigator’s Brochures (IBs)
Investigational New Drug Applications (INDs)
Clinical Trial Protocols
Informed Consent Forms (ICFs)
Clinical Study Reports (CSRs)
Clinical Manuscripts, Abstracts, and Posters
Nonclinical and Clinical Overviews (NCO/CO)
Publications and Scientific Writing
Manuscripts & Journal Articles
Abstracts
Posters
Slide Decks & Scientific Presentations
Literature Reviews
White Papers
Clientele
We partner with teams and organizations across the life sciences ecosystem that value expertise and reliability. Each of our client types share a common goal: to advance novel therapies with precise, compliant scientific communications.
Pharma & Biotech Companies
developing novel oncology and immunology drugs to advance their pipeline.
CROs & Clinical Operations Teams
providing regulatory and clinical development support to collaborators and sponsors.
Academic Institutes & Research Centers
conducting translational or clinical research in oncology and immunology.
Medical Writing Agencies
seeking writers to deliver accurate, high-quality documents for their clients.
Our Approach
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We start with an introductory call to review your project needs and put any necessary contracts into place.
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We develop a clear scope of work with defined objectives, timelines, responsibilities, communication plans, project milestones, and pricing.
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We gather study data, background documents, and literature to build a solid evidence base and create a tailored outline.
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We prepare the first draft based on the established outline using clear, scientifically sound language.
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Each draft undergoes project team review and we consolidate feedback, resolve queries, and apply necessary revisions or amendments.
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We check formatting, prepare the document for submission, assist with submission, and address follow-up queries.