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:

  1. Expertise to tackle your medical writing requirements in compliance with  FDA and WHO
  2. Convincing medical content for consumers and medical experts.
  3. Engaging and informative  documents designed to achieve the goal with comprehensive market strategy.
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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.

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  1. Communication with wide range of audience
  2. Complete, end-to-end communications services at development and commercialization
  • Clinical trial publications
  • Market access
  • Publications planning
  • Medical and scientific education
  • Patient communications
  • Regulatory documents
  • Preclinical research reports:
  • Clinical data and literature summaries
  • Clinical Protocols
  • Clinical Protocols
  • Post-marketing documents
  • Consumer medicine/device information
  • Grant writing
  • Clinical Research Publications
  • Case reports
  • Case series
  • Cohort studies

Key Features

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

Work Gallery

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GET IN TOUCH

Email:

[email protected]

Phone:

+91-9811631059

Location:

Bangalore, Karnataka India

North East Ham, London UK

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