In Clinical trials, the medical writers serve as a crucial bridge in defining the strategies and goals of a clinical study to the patients, regulatory agencies and sponsors. Therefore, a medical writer should have a clear grasp of the medical terminologies and ideas. Our writing team works in coordination with our QA team, data management team and other team’s part of a project to create the necessary documentation for clinical trial projects.
At Manentia, our experienced team provides well-written, proficient, flexibility and timely documentation for your product development efforts by delivering high-quality services. Our qualified team of writers and editors has vast experience in managing medical content.
Based on the document needs of our clients, we create documents that demonstrate excellent language usage, clear communication, and adherence to scientific writing standards. Ranging from the informed consent document to the advanced protocol or a newly launch drug application, the team makes sure to thoroughly cross-check every minute details according to the regulatory compliance.
Medical Writing Services Include:
- Clinical trial protocols development
- Investigator brochures
- Journal Manuscripts
- Research Proposals
- Systemic literature reviews and critical analyses of new drugs, therapeutic areas, and competitive analyses
- Informed consent form drafting
- Documents pertaining to execution of clinical trial like patient diaries, templates for documentation etc.
- Clinical study reports.