InClinition

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.



Translation services

We offer translation services in Indian languages for informed consent document in clinical trials



Regulatory Support

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



Publication Services

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



Pharmaceuticals

Formulation Development

Analytical Development

Process Development

Technology Transfer



Operational Assistance

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



Office support

Back Office and business office Support

Feasibility Assessments

Organization of Meetings