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)


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


  • GMP, GCP, GLP Audits

  • Formulation Development

  • Analytical Development

  • Process Development

  • Technology Transfer


Pharmaceutical Process Engineering and Allied Services

We provide following solutions to allopathic, homeopathic, ayurvedic, nutraceuticals and biotechnology industries.

  • GMP Compliance

  • Product Quality Improvement

  • Cost Reduction

  • Documentation Systems Support

  • Process efficiency improvement

  • Improvement of product output

  • Energy conservation

  • Labour reduction

  • Infrastructure setup

  • Machine design, selection, erection and commission

  • Air Handling Units (AHU) services

  • Machines, Packing systems, Raw materials sourcing

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