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Medical Writing
Medical writers at Clinexa understand that well written clinical trial documents are an extremely important link in the whole process of clinical research. At Clinexa, teams of efficient and experienced medical writer’s are diligent to provide our client with documentation that will help to realize their regulatory and marketing goals. We have proficiency to communicate complex clinical data in a concise and unambiguous manner.

Clinexa offers writing services for whole clinical trial development program and provides a full range of documents from regulatory to scientific and medical domain. We use client’s templates or our own ICH based ones as per the requirement, thus following greatest flexibility.

Some of our medical writing deliverables are:
    Pre-submission documentation::
    Clinical study protocol
    Investigator brochures
    Patient informed consent forms
    Investigational New Drug Application (IND)

    Post-submission documentation::
    Clinical study report (CSR)
    Integrated summary of safety and efficacy
    Common technical documents (CTD), other formats
    Premarketing and post-approval annual reports
    Phase I-IV integrated clinical statistical reports (ICSR)

    Scientific / medical communication::
    Literature reviews
    Posters, abstracts, and manuscripts
    Educational material
    Marketing and training material

Content Development & Article Writing Service
Clinexa Life Sciences has a team of experienced content developers and medical writers who can easily cater to any volume of work and turnaround times. Turnaround times for rewritten articles can be as per expectation of the client. Clinexa has the capability to return rewritten content in less than 24 hours.

All content is written by experienced medical writers who have good command of English language, understanding of google SEO and know the importance of keyword rich content.

The overall management of all medical writing and content development services is the responsibility of a Senior Medical Writer at Clinexa. The Senior Medical Writer works closely with the team of experienced medical writers and project coordinators (PC’s) assigned to the project.

Medical writers are responsible for all day-to-day writing requirements including editing, writing and proof reading of content. Medical writers ensure that rewritten content is keyword rich and unique so that the clients benefit the most in terms of Search Engine Optimization (SEO). It is the responsibility of Clinexa project coordinators to ensure that all content is run through copyscape and other in-house plagiarism softwares to ensure that the content is unique before it is delivered to the clients.

In addition to providing high quality service to its valued clients, Clinexa offers highly competitive hourly rates or per word count rates depending on the volume of work. Clinexa aims to be looked upon as a partner that provides high value for every dollar spent by its clients.

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