Artem Nova
The success of a clinical development program ultimately depends on the presentation and understandability of documents. Crafting clear, concise, and accurate documents with compelling key messages is an Art.
At Artem Nova, medical writing is our art. As specialists in clinical, regulatory, and scientific documentation, we deliver strategic, accurate, and timely documents of the highest quality.
Our medical writing expertise spans all major therapeutic areas and stages of development. We tailor our medical writing services to meet client needs, serving pharmaceutical and biotechnology companies of all sizes, worldwide.
About Us
Dr. Leslie Chu is the Founder of Artem Nova LLC, with over 20 years’ experience in regulatory writing and scientific communications. She holds a PhD in Biomedical Sciences and is RAC certified.
Dr. Chu has consulted for over 65 pharmaceutical and biotechnology companies. She has extensive experience in small molecule, biologic, and device development. Dr. Chu brings her broad medical writing expertise and strong understanding of regulations to craft and hone preclinical, clinical, regulatory, and scientific documents and communications. She is a creative and adaptable project manager, with a steadfast commitment to excellence.
Our Services
Boost your drug, biologic, or device to the next stage of development with
Artem Nova's Regulatory and Clinical Writing Services.
Optimize how you inform the world about your advances in drug, biologic, or device development with Artem Nova's Scientific Writing and Communication Services.
Why Choose Us
Artem Nova has helped over 65 pharmaceutical and biotechnology companies achieve their clinical development goals.
Regulatory documentation and scientific communication are critical to the success of clinical development programs. Drug approval and marketing ultimately depend on clear, concise, and accurate documentation.
Artem Nova partners with you to create compelling and clear documents that boost your program to the next phase of development.
We work with you as integral team members, providing proactive project planning, document creation, and document life-cycle management, with a commitment to timeliness and excellence. We have been privileged to serve over 65 pharmaceutical and biotechnology companies of all sizes, worldwide, for over 20 years. If you are looking to produce the highest-quality documents on-time and in-budget, contact us.
We have partnered with AI developers to create initial drafts of clinical study documents in just 5 days. Using our AI-powered medical writing tool, we can generate your clinical study protocol, informed consent form, study procedures manuals, and start-up checklists simultaneously.
Get Started
Chat with us and let’s discuss how we can support your clinical documentation needs!
Thank you for considering Artem Nova. Contact us today to discuss your needs.
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