We offer medical writing services from beginning to end in six primary areas:
- Scientific & Academic Writing: Writing manuscripts, literature reviews, systematic reviews (PRISMA), meta-analyses, case reports, grant writing, and experimental designs.
- Regulatory Medical Writing: Writing protocols, CSRs, CTDs, CERs, IFUs, risk-benefit analyses, and post-market surveillance documents.
- Pharma & Biotech Content: Writing product dossiers, white papers, MSL slide decks, briefs for document updates, and investor documents.
- Medical Device & Digital Health Writing: Writing clinical evaluation reports (MDR/IVDR), SaMD documentation, validation summary documents, and software IFUs.
- Commercial & Patient Communication: Writing patient education documents, HCP brochures, medical marketing content, and digital content.
- Editorial & Quality Support: Medical editing, formatting, referencing, plagiarism checks, and journal submissions.
- Bonus Services include writing visual abstracts, scripting scientific animations, and data for AI validation documents and pitch decks.
Deliverables will vary, based on service type, but may include:
- Well supported scientifically sound documents that do not have plagiarism and have others correctly cited
- Clear identification of gaps in research, controversies in literature and clearly identified problems statements
- Formatted document that meets journal, regulatory or company specifications- Along with aligned research objectives, frameworks also for manufacturers on premium plans including custom formatting for expedited acceptance or approval.
Yes! You can choose from the Standard, Advanced, and Elite tiers at different levels of depth, support, and complexity. The plans are across all tiers and include:
- Citation style (AMA, APA, Vancouver, etc.)
- Full scientific research articles with statistical support
- Strategic regulatory writing following compliance review
- Scientific storytelling and commercialization-ready content
To preserve precision and uniqueness, please provide:
- Field/domain (e.g., clinical research, digital health, biotech
- Country/region focus (e.g., UK, US, EU, GCC)
- Target audience (e.g., journal, regulatory body, HCPs, patients)
- Research purpose or study proposal
- Example sources or preferred references
- Institutional or publication guidelines
- Academic background, specialization, and supervisor’s area (for author support)
All writers hold master’s degree or PHD in life sciences or medicine or pharmacy and have 5+ years of experience in the field. Writers are assigned to write based on their therapeutic area of specialization for maximum depth of knowledge, ensures depth of regulatory regulation, and clarity and consistency. We recruit internationally (UK, EU and APAC) and guarantee alignment with subject-matter experts for each project. All writers hold master’s degree or PHD in life sciences, medicine, or pharmacy with 5+ years of experience in their field.
Once confirmed, your project is given to a Project Associate (PA), who will read your brief and clarify your instructions, if necessary. A subject-matter expert will be assigned to your project after signing an NDA.
The project process includes:
- Technical writing and review
- Internal Quality Assurance (QA) checks
- Plagiarism checks
- Final delivery with QA and plagiarism reports
We provide a satisfaction guarantee based on:
- On-time delivery
- Plagiarism-free, original work (typically <5-10%)
- With all details consistent with the scope and brief
- Domain-expert assignment
If any of these cannot be fulfilled, we revise or rework the content based on our revision policy. Refunds might be considered only when critical and agreed-upon service guarantees are unfulfilled, subject to the terms.
- Plagiarism-checked (<5%)
- Qualified domain-specific writers
- Timely delivery
- Scientifically, and structurally accurate writing
- Confidentiality and intellectual property protection
- Journal, or governmental regulations compliance
Every piece of writing is completed by vetted, experienced in-house and extended network professionals – who are all bound by confidentiality. We never sacrifice quality or subject familiarity. Our in-house QA and editorial team ensure consistency and quality in every project.
We also support the entire process; writing, reviewing, visual assets, and submissions – we are a complete medical writing partner.
Yes. Our regulatory and clinical writing is always informed by ICH (International Council for Harmonisation) and GCP (Good Clinical Practice) regulations. Whether we are writing CSRs, protocols, or informed consent documents, we assure the regulatory compliance worldwide and scientific integrity.
Yes, our medical writers are knowledgeable about the EU MDR requirements, including Clinical Evaluation Report (CER) structure according to MEDDEV 2.7/1 rev. 4, as well as Annex XIV Part A. We use compliant CER templates and apply the best practices in accordance with the MDCG guidelines (for example, MDCG 2020-7).
Yes, we take confidentiality to heart. Every project starts with a Non-Disclosure Agreement (NDA) so that we can protect your intellectual property, unpublished data, and proprietary information. All writers and project managers are bound by internal confidentiality agreements.
