Let Veristat Do the Medical Writing for You
Whether you are…
- Starting to plan your trial and need a protocol written
- Mid-study and need more writing resources
- Under a time crunch to get your regulatory submission finalized
Veristat can help keep you moving forward.
Medical Writing Expertise
Veristat’s medical writing team members have strong scientific backgrounds and a wide range of therapeutic area expertise.
Veristat offers a core expertise in writing all clinical trial and submission documents including:
- Global Regulatory Documents in eCTD Format – INDs, NDAs, IMPDs, MAAs
- Regulatory Briefing Documents
- Clinical Study Protocols
- Clinical Study Reports (CSR)
- Investigator Brochures
- Patient Safety Narratives
- Risk Management Plans
- Annual Report Writing
In addition to the common types of clinical trial and submission projects, we can also help your teams with other writing projects such as:
- Clinical Trial Registration & Results Postings on ClinicalTrials.gov
- White Papers to Supplement Submissions
- Literature Reviews
- Abstracts, Posters, & Manuscripts for Scientific Meetings
Veristat can help with any writing project that you have.
Schedule a Meeting
Tell Veristat about your current medical writing challenges. Contact us today!