medical writing
experienced clinical professionals
Our Clinical Consultants are skilled Medical Writers with a broad range of device experience.
medical writers
Our Medical Writers are Clinical professionals with a broad range of expertise including:
- Technical Writing
- Submission Authoring
- Clinical Documents creation
- Product Surveillance documentation
- Clinical Analysis and Reporting
- Clinical Abstracts
- Manuscripts support
- Study Brochures
- Marketing Documentation and Review
specialized medical writing services
Whether you are looking for support with clinical study documentation or planning on submitting a new product we have the expertise to support you. Are you looking for support in any of the following:
- Clinical Documentation Templates
- Support with Submissions
- Briefing Books
- Clinical Development Plan (CDP)
- Clinical Study Protocol (CSP)
- Clinical Study Report (CSR)
- Common Technical Document (CTD)
- Informed Consent Form (ICF)
- Investigator’s Brochure (IB)
- Investigational Medicinal Product Dossier (IMPD)
- Investigational New Drug (IND)
- Pediatric Investigation Plan (PIP)
- Responses to Authority Clinical Questions
- Clinical Evaluation Reports (CER)
- Post-Market Surveillance Report
- Clinical Analysis
- Summary of Safety and Clinical Performance (SSCP)
CLINICAL AND REGULATORY SOLUTIONS
Our Medical Writers bring a broad range of expertise within Clinical and Regulatory compliance. We focus in a solutions based approach for the entire lifecycle of the device or drug.
Interested in our services? We’re here to help!
We want to know your needs exactly so that we can provide the perfect solution.
