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Summary

Preclinical Expertise and Regulatory Medical Writing is an excellent contribution to your drug discovery and development process.

Sylvia Lemstra – your life science professional – will add quality to your preclinical and clinical projects.

Contact

Sylvia Lemstra, Freelance Medical WriterM.Sc. Medicinal ChemistryB.Sc. Analytical Chemistry

Phone: +49 (0)89 189 23 161 Mobile: +49 (0)179 387 36 35

info@slmedicalwriting.comwww.slmedicalwriting.com

Writing for Life Science

Services

Expert knowledge at the right time keeps pace in the process. Strengthen your team with a regulatory medical writer who is an expert in drug discovery and development.

SL Medical Writing Delivers High quality preclinical reporting with

visualization of complex data

Regulatory medical writing (CSP, CSR, IB, IND)

Scientifi c manuscript preparation

Preclinical study management

Expert contribution to drug discovery and preclinical development plans

Writing for Life Science

My freelance business, SL Medical Writing, is active since 2014 and sources from experience in different scientifi c roles in pharmacology and preclinical development since 1998. I know that lab work is sometimes a great and costly endeavour which is absolutely worthy of decent do-cumentation. Only documented science has value, because only then it is accessible and usable.

At SL Medical Writing you will fi nd writing and editing expertise in Investigator’s Brochures (IB) Investigational New Drug dossiers (IND) Clinical Study Protocols (CSP) Clinical Study Reports (CSR) PK and PD Reports (preclinical and clinical) Scientifi c Publications

My sound industry experience in pharmacology and preclinical development can additionally sup-port you in regulatory safety and toxicity studies. Also effi cacy and proof-of-concept studies, DMPK and PK/PD concepts are part of my scientifi c knowledge. My medical fi eld expertise includes immunology and oncology.

Mission

My mission is to create life science documents that are understandable and accessible to a scientifi c, regulatory or lay audience.

Writing QualitySL Medical Writing turns your data into expert reports, scientifi c publications and regulatory documents, making sure your science is under-standable and accessible.

SL Medical Writing is dedicated to deliver high quality documents. This means that scientifi c texts are accurate, clear and concise; scientifi c information is consis-tent throughout the dossier; report synopses are well written and can be used in many regulatory documents; and graphs transport the key message at fi rst glance. Well written scientifi c information leaves a persuasive impression of your dossier.

Service-oriented, Reliable, Scientifi c

If you want your dossier to be persuasive with structured, accurate, legible, clear and concise information, I am your fl exible and service-oriented partner.

If you want to structure your project to comply with regulatory requirements for preclinical and clinical phase I/II trials, I am your reliable and EMWA-certifi ed regulatory medical writer.

If you want to address key features in your target product profi le such as mode of action, pharmacokinetics, regulatory safety and toxi-city to complete your preclinical package, I am your experienced scientist.

With SL Medical Writing on your team, not only your science will be clear and accessible, you will also benefi t from key knowledge of Pharma-cology, Pharmacodynamics, Pharmacokinetics, Toxicology and the appropriate use of regula-tory guidance.

Teaming up with SL Medical Writing adds quality

to preclinical and clinical projects.

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