Our services are tailored for physicians, surgeons, clinician-researchers, PhD scholars, postdoctoral fellows, medical faculty, and industry-sponsored investigators preparing proposals for IRB submission, grants, or academic approvals.
We understand your schedule. After the initial consultation and document handover, we manage the drafting process with minimal time required from you. You’ll review the draft at key milestones, with a dedicated coordinator guiding you throughout.
Yes. We strictly adhere to the formats required by universities and funding agencies like ICMR, DBT, DST, NIH, ERC, Horizon Europe, and private foundations. We also accommodate institutional and hospital-specific ethics board guidelines.
A typical document includes:
- Title, abstract, and background
- Literature review and identification of the research gap
- Objectives and hypotheses
- Study design and methodology (including sample size, tools, statistical plan)
- Ethical considerations
- Expected outcomes and significance
- References and proper formatting
- Informed consent forms
- Participant information sheets
- Risk–benefit assessment
- Data handling/privacy compliance (e.g., HIPAA/GDPR if required)
Yes. We specialize in protocols for surgical interventions, device studies, and procedural innovations. Our team ensures compliance with applicable clinical investigation standards (e.g., ISO 14155 for devices).
- Budget estimation and justification
- Timeline or Gantt chart
- Evaluation metrics and impact summary
- Funder-specific formatting
Yes. You retain full authorship and intellectual ownership. We work as your scientific support team, and all contributions comply with ICMJE authorship guidelines.
Yes. We sign NDAs upon request, and all files and communication are handled securely. Your data, research concept, and authorship rights are fully protected.
- Basic: 10–12 business days
- Advanced: 12–15 business days
- Premium: 15–20 business days