Medical Writing Consulting Services
Your drug-development story is important. Let our experts help you craft it.
Engaging experienced medical writing consultants early in the drug development process can help you avoid costly delays and accelerate approval.
We dedicate a specific team of medical writers to each client, so we can work as a true extension of your team. Our medical writers average more than 18 years of experience, and the majority have earned advanced degrees. Our team has authored more than 100 clinical study reports, more than 250 common technical document (CTD) summaries and more than 100 clinical study report (CSR) summaries. And we haven’t missed a single project milestone in the past 10 years.
We specialize in medical writing for clinical research, so we can quickly summarize complex data into concise, accurate reports, in formats that comply with regulatory requirements.
Our medical writing services team has expertise in all major therapeutic areas and all stages of development. We work with all product types, ranging from small molecules to biologics and biosimilars. Our quality medical writing solutions can be customized to serve clients of any size – from small, virtual biotech firms to global pharmaceutical companies. And our internal controls ensure we deliver quality clinical documents, on deadline.
Get it “write” the first time
Learn how a dedicated team of experienced, quality medical writers can get your product to patients, faster. Contact us today.