
Medical writing
Our mission is competent, effective and on-point medical-scientific communications. The term medical writing covers a wide range of services and fields: from writing informational texts for the general public to drafting manuscripts for scientific papers intended for publication in peer-reviewed journals. But also regulatory writing, the organisation and reporting of advisory boards and the production of content for newsletters or corporate websites.
We have the right person for your message.
Medical writing services for scientific research
Our medical writing services for the world of biomedical research include:

Submission to peer-reviewed journals

Bibliographical research

Preparation (including graphics) of abstracts, posters and slide kits

Linguistic revision of scientific English
Advisory boards and medical-scientific events
We organise advisory boards in any therapeutic field, both in-person and online. Our medical writers support you in writing a reasoned and concise report, and also act as moderators of the event, if requested. The report can be written in Italian, English or any other language required. If necessary, we can support you with interpreting services in any language.
We help you to devise the best format for your advisory board or event in order to make it more productive and facilitate output, be it a report or any other product.
We help you to organise event logistics, manage the budget and find the best solutions for carrying out the event. We also take care of the graphics and printing of promotional and informative materials, as well as media such as animations, and the creation and editing of event videos (speaker interviews, video clips, etc.).
Regulatory writing services
ASTW offers its clients regulatory writing services combined with English-language editing of the documents produced. The aim is to provide customers with technically and linguistically flawless regulatory documents.
We can provide the following regulatory documents:
Clinical documentation
Clinical Development plan
Clinical Study Reports (CSR)
Common Technical Documents (CTD)
Investigator’s Brochures (IB)
Investigational New Drugs (IND)
Pediatric Study Plans (PSP)
Lay Summaries
Clinical Study Protocols (CSP)
Investigational Medicinal Product Dossier (IMPD)
Clinical Investigation Plans (CIP)
Informed Consent Forms (ICF)
Pediatric Investigation Plans (PIP)
Clinical Evaluation Plans (CEP)
Clinical Evaluation Reports (CER)
Periodic Safety Update Reports (PSUR)
Risk Management Plans (RMP)
Post-Market Clinical Follow-Ups (PMCF)
Regulatory intelligence reports
Summaries of safety and clinical performance (SSCP)

Other services
We believe that the value for the customer is finding several solutions in a single place. Alongside medical writing services, ASTW also offers services such as: