Get Medical Writing Services by a Top-Rated Medical Writer
Work with a registered pharmacist on journal manuscripts, literature reviews, systematic review and meta-analysis support, drug safety and pharmacovigilance documents, regulatory writing, CMC content, patient education and CME/CPD materials.
Healthcare, pharmaceutical, medical device, digital health and medical education experience.
My medical writing experience spans healthcare, pharmaceuticals, medical devices, digital health and medical education, including current engagements with Sinocare, Cardinal Health and OMT Training, as well as selected projects for IT Medical, AmplifyMD, Airgas Therapeutics and Constant Therapy Health.
These projects have covered patient education, medical communications, healthcare white papers, healthcare professional materials, manuscript development, regulatory writing, scientific communication, literature review and publication-focused editing.
Medical writing services for scientific publications, medical communications and healthcare content.
Choose the level of medical writing support your project requires. Services may include white paper writing, literature review, manuscript development, scientific editing, reference management and CME/CPD materials development.
Manuscript and publication support
For clinicians, researchers and academic teams preparing work for peer-reviewed journals.
- Original research manuscripts
- Case reports and clinical case series
- Journal formatting, cover letters and reviewer responses
Literature reviews and evidence synthesis
For projects that need structured literature searching, critical appraisal and clear synthesis.
- Narrative reviews and systematic review support
- PICOS, search strategy and screening support
- PRISMA flow diagrams, risk of bias assessment and narrative synthesis
Pharmacovigilance and drug safety writing
For pharmacovigilance, drug safety and regulatory teams that need accurate safety-focused documents.
- Benefit-risk assessments
- Adverse event and serious adverse event narratives
- Safety communications and pharmacovigilance SOPs
Regulatory and CMC content
For pharmaceutical, regulatory affairs and medical device teams that need clear scientific and technical content.
- CMC and quality-related articles
- Regulatory summaries and scientific writing
- Healthcare white papers and professional medical content
Patient education and medical device content
For medical device and healthcare brands that need plain language health information with medical accuracy.
- Diabetes education and blood glucose monitoring content
- Patient-facing articles and educational materials
- Medical device education and product information content
Medical education and training materials
For teams turning medical evidence into CME, CPD, teaching or training content.
- Clinical slide decks
- Speaker notes and evidence summaries
- Learning modules and teaching materials
A specialist area few medical writers can cover.
In addition to regulatory writing and peer-reviewed manuscript development, I have extensive experience in manual therapy content, an area in which few medical writers have genuine authorship credentials. I have an ongoing collaboration with manual therapy author and educator Giles Gyer, covering books, peer-reviewed publications and CME/CPD materials.
Co-author of a critical literature review on the biomechanical parameters of spinal manipulation, published in the Journal of Integrative Medicine in 2022.
Contributed as a ghostwriter to six manual therapy books covering spinal manipulation, foot and ankle manipulation, osteopathic and chiropractic techniques, dry needling and the Gonstead technique.
Developed CME and CPD teaching materials for manual therapy practitioners, including high-velocity, low-amplitude (HVLA) techniques, cervical manipulation safety and dry needling.
Defined deliverables for each project scope.
Send me the details about the project type, audience and source material. I will define the deliverables, source requirements, timeline, review rounds and limits before work starts.
Manuscripts, case reports, abstracts, cover letters, journal formatting, reference checks and reviewer response documents.
Search strategy notes, screening support, data extraction tables, risk of bias assessment, PRISMA flow diagrams and narrative synthesis drafts.
Pharmacovigilance summaries, benefit-risk assessments, adverse event narratives, safety communications, pharmacovigilance SOPs, CMC articles and regulatory summaries.
Healthcare white papers, evidence-based articles, website copy, patient education, medical device content and digital health content.
CME and CPD slide decks, learning modules, speaker notes, evidence summaries and teaching materials.
A good fit when accuracy, evidence and audience matter.
A general writer can improve style. A medical writer helps maintain scientific accuracy, clinical meaning, reference integrity, claim substantiation and audience suitability. That is where I add the most.
A simple process for serious work.
The first step is a project brief. That makes scope, timing, deliverables and cost easier to judge before either side commits.
You send a brief
Project type, audience, deadline, target journal or platform, word count and the source material you have.
I check fit
I review the scope, evidence needs, timeline, claim substantiation needs and whether I can genuinely add value. You hear back within 24 hours.
You get a quote
A clear quote with deliverables, price basis, timeline, review rounds and any questions, before work begins.
We build the draft
You receive a structured draft, agreed revisions and a clean final document prepared for the intended journal, platform or audience.
Clear answers on fees, scope and publication limits.
A short edit, a patient education article and a full manuscript do not require the same research, writing or review. Fees follow the scope.
How much will it cost?
Fees depend on scope, deadline, research depth, source material, reference work and review rounds. A short edit may start around $100. Full manuscripts, reviews, white papers and regulatory projects are quoted after I review the brief. You always get a detailed quote before any work starts.
What affects the quote?
Project type, word count, deadline, available source material, literature review needs, reference work, review rounds and formatting requirements.
Can I get a quote before I am ready?
Yes. Send the brief even if the project is not final. You will get a clear read on fit and likely scope, with no obligation if you postpone or cancel.
How do we work together?
By email, Zoom, Google Meet, Skype or WhatsApp. Contracts can run through Upwork, PeoplePerHour or Kolabtree, or directly using a mutually suitable payment method.
Can you guarantee publication?
No. Journal acceptance depends on editorial assessment, peer review, study design, data quality and journal scope, which no writer controls. I can improve structure, reporting, clarity, references, journal formatting and reviewer responses within agreed revision rounds.
Do you work with individual researchers?
Yes. Researchers, clinicians and students are welcome, not just companies. The requirements are the same: a clear scope, appropriate source material and a reasonable timeline.
Pharmacy background and publication-focused writing.
My pharmacy background helps me interpret mechanisms of action, drug safety data, clinical claims and drug information with the level of caution medical content requires. I can support literature searching, manuscript development, scientific editing, reference management, journal formatting and reviewer responses within one coordinated workflow. My longest client engagement runs 11 years and several clients have returned for five or more projects.
Clinical research and scientific writing training.
Relevant certificates, each verifiable:
Pharmaceutical industry background.
My professional background combines pharmacy and pharmaceutical industry experience. I hold a Bachelor of Pharmacy from Stamford University Bangladesh and am a registered pharmacist with the Bangladesh Pharmacy Council (BPC). Before moving into freelance medical writing in 2011, I worked in quality control, pharmaceutical production and product development, gaining practical experience in drug development, cGMP documentation, manufacturing operations and safety communication.
What clients say after working with me.
The strongest signal a writer can give is a client who comes back. Short excerpts below. The portfolio page carries the full testimonials.
Imtiaz is my go-to writer. I cannot rate him highly enough!
He stood out as one of our best writers for his mastery of the English language, attention to detail and deadlines.
References were directly on target. Formatting was perfect. Timeliness was even better than the unreasonable goal I requested.
Excellent work! Quick research and reporting on a science intense data research and collection.
Imtiaz did a fantastic job for us. He is very thorough in his work and brings a lot to the table in planning the articles.
They were well researched, written and referenced. He has a good medical knowledge.
Easy to check before you reach out.
The portfolio shows publications, evidence synthesis projects, book work, healthcare content samples and client-owned work summaries. My ratings, reviews and publication records are open on the profiles below.
Send a short project brief.
You do not need a polished brief. Share the available details you have, and I’ll let you know whether I’m the right fit, what I need and how the project can be structured. I’ll respond within 24 hours.