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.
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
Company incorporation in India
Setting up branch office in India
Regulatory and Statutory Compliances
Legal Advisory on Indian Corporate and Commercial Acts/Laws
Manpower Recruitment and Other Support Services
Dedicated Technical or Administrative Representative
Back Office and business office Support
Organization of Meetings