• High quality preclinical reporting with visualization of complex data
• Regulatory medical writing (CSP, CSR, IB, IND)
• Scientific manuscript preparation
• Preclinical study management
• Expert contribution to drug discovery and preclinical development plans

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!

Service oriented, Reliable, Scientific

• If you want your dossier to be persuasive with structured, accurate, legible, clear and concise information, I am your flexible 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-certified regulatory medical writer.

• If you want to address key features in your target product profile such as mode of action, pharmacokinetics, regulatory safety and toxicity 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 benefit from key knowledge of Pharmacology, Pharmacodynamics, Pharmacokinetics, Toxicology and the appropriate use of regulatory guidance. Strengthen your team with my profound insight in drug discovery and development processes.