Medical and Regulatory writing
- Development of essential documents for clinical trial (Protocol, ICF, IB, CRF etc).
- Preparation of manuscripts, abstracts, posters, research communications etc.
- Preparation of CSR and other study reports.
- Preparation of product monographs
- Leave behind literatures (LBL)
We offer translation services in Indian languages for informed consent document in clinical trials
- Guidance on Indian Clinical Trial Regulations
- Informed Consent Document (ICD) as per Indian regulatory requirements
- Dossier preparation, submission and liaison for Trial Permissions, Import and Export Licenses etc.
- Reporting of Adverse events
- Manuscript editing, writing, reviewing
- Preparation of presentations, posters for conferences
- Publication assistance for publishing in different journals (journal selection, submission, review, correspondence, proof editing, etc.)
- Writing conference proceedings and publishing them.
- Over layering of spectra, figures artwork services
- Statistical analysis for publications
- Research and grant proposal writings