Medical Writing
Our team of expert medical writers provides medical writing services that helps you communicate your results to the scientific community, funding agencies, regulatory bodies, and the general public in a clear and meaningful way.
This service is relevant for :
Our regulatory medical writing service can improve a wide variety of regulatory documents, including clinical evaluation reports, orphan drug designation (ODD) applications, briefing documents, pre-investigational new drug (pre-IND) meeting requests, clinical trial applications, and clinical trial reports
Medical Device
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Clinical development plans (regulatory strategy, part of clinical evaluation plan)
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Clinical investigation application
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Clinical investigation notification
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and more—ensuring complete documentation support
Pharmaceutical
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Clinical trial applications (via the clinical trial information system (CTIS)
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Clinical trial protocols
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Clinical trial reports
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Investigator brochures
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and all other essential documents—comprehensive support from start to finish
Regulatory
Medical writers significantly improve the quality of regulatory documents. Our expert medical writers help ensure your regulatory documents are clearly written and appropriately formatted, letting you focus on your regulatory strategy. We can help find supporting literature for your scientific and regulatory positions and to establish the background and state of the art in a particular therapeutic area, as well as provide medical writing services, language editing, and formatting of documents.
How we work
01
Book a Free Consultation
Contact us to schedule a free 30-minute consultation to determine which services will best help you.
A nondisclosure agreement is signed before consultation to protect your ideas and data.
02
Nondisclosure Agreement
We value your confidentiality. Before any project begins, both parties sign an NDA to ensure all shared information remains secure and private.
03
Quote & Service Agreement
After your consultation, you'll receive a detailed quote and sign a service agreement outlining the project scope and deliverables. Each project is assigned a research consultant and a medical writer who will work closely with you to develop an outline and maintain scientific quality.
04
Consultant & Medical Writer Collaboration
Your dedicated consultant and medical writer collaborate with you throughout the process, refining content and ensuring the document meets your goals and standards.Additional services such as journal selection, figures, and illustrations can be included at this stage.
05
Native English Medical Writer Drafts Your Document
A native English-speaking medical writer crafts a clear, accurate, and well-structured document that effectively communicates your research and findings.
Get in touch
Need support with grant application?
Have a complementry coffee on us over a quick chat
What our Clients values the most
Expertise
>12 years of experience in translational and biomedical research.
Quality
Attention to detail, high standards, and a commitment to make a difference.
Flexibility
Flexible collaboration tailored to your goals, timeline, and resources.
Testimonials
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Simone Woods
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Nicole Yang
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Calvin Smith
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Suzanne Levis
Our Services
Supporting Services
Life Science Startups, Academia
Medical Writing
Life Science Startups
Clinical Project Management
Life Science Startups, Academia
Where you can find us
Address
Medicon Village, Scheelevägen 1, 223 63 Lund
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