Working closely with the statistical, medical, regulatory and data management teams, our medical writers deliver meticulously accurate, timely and cost-effective documents to the highest ethical and scientific standards
Medical Writing
Our medical writers have a wide depth of knowledge and experience drawn from the pharmaceutical industry, contract research organisation and academic research. All documents produced by Quanticate undergo thorough scientific, statistical,
editorial and quality control review.
Quanticate’s medical writing services include clinical and regulatory writing as well as scientific communications, education material and medical writing consultancy. Examples include:
- ICH-GCP compliant Clinical Study Reports; Phases 1 to 4, Including Clinical Study Report Synopses for Public Disclosure
- Protocols
- Clinical and Non-Clinical Sections of the Common Technical Document (CTD) Including Summaries and Overviews for EU or US Regulatory Authorities
- Investigator Brochures
- Patient Safety Narratives
- Patient Information Including Informed Consent and Patient Brochures
- Periodic Safety Update Reports
Scientific Communications
- Publication Planning
- Conference Material (abstracts, poster presentations and slide sets)
- Manuscripts
- Editorial Support
- Journal/Conference Submission
- Product Website Content (for both scientific and patient audiences)
- Educational Material for Patients, Healthcare Professionals and Pharmaceutical Industry Personnel
- Medical Marketing Reviews and Reports
- Literature Reviews
