An efficient, research orientated, and single-source solution to all medical writing requirements
Medical writing is considered to be complex but we aim to provide your research, products and services to individuals in precise, engaging and simple form. We deliver high quality documents across the clinical development stages and minimize time to market through efficient, accurate, and compliant documentation.
Here we provide:
Expertise to tackle your medical writing requirements in compliance with FDA and WHO
Convincing medical content for consumers and medical experts.
Engaging and informative documents designed to achieve the goal with comprehensive market strategy.
Well drafted medical content in compliance with reporting guidelines
We strongly follow standard guidelines as
COPE (committee on Publication Ethics)
Provides guidelines for publishers, journals and editors.
EQUATOR (Enhancing the Quality and Transparency Of health Research)
Guidelines for reporting health research
ICMJE (International Committee of Medical Journal Editors)
Guidelines for research publications in Medical Journals
GPP (Good Publication Practice)
Guidelines for publishing clinical trials.
Communication with wide range of audience
Complete, end-to-end communications services at development and commercialization
Clinical trial publications
Medical and scientific education
Preclinical research reports:
Clinical data and literature summaries
Consumer medicine/device information
Clinical Research Publications
Assistance in clinical research design and proposal development for diverse studies across varying medical indications
Ensuring that documents are clinically relevant and literature supported
Reviewing various clinical and regulatory documents
Integration of appropriate data into clinical protocols, investigator brochure, clinical study reports, and other clinical and regulatory documents
Ensuring standardization of all clinical documents according to templates, and maintaining quality and consistency of documents throughout
Writing, editing and revising grant applications including HHS BARDA, NIH, and NSF