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Ethics-Ready Study Design

Research Protocols & Study Planning

Transforming clinical concepts into methodologically sound, funder-aligned protocols ready for Institutional Ethics Committee (IEC) submission and trial registries.

Clinical Research Protocol Design
Methodology & Justification

Exhaustive Literature Audit & PICO Framework

Ensure your clinical research idea possesses genuine novelty, ethical justification, and high publication feasibility before investing clinical resources. Our senior research methodologists evaluate PubMed, Scopus, and Cochrane databases to formulate razor-sharp research objectives.

PICO / FINER framework hypothesis validation
Primary and secondary endpoint formulation
Institutional Ethics Committee (IEC) documentation
Sample size calculation with 80%–90% statistical power

What is Included in the Protocol Package

Every protocol deliverable is audited by senior faculty under strict bilateral NDA.

Novelty Scorecard

Literature gap analysis with target journal recommendations and impact scorecard.

Sample Size Estimation

Mathematical formulation based on anticipated effect size, alpha error, and beta power.

Ethics Protocol Draft

Complete background, methodology, inclusion/exclusion criteria, and patient consent template.

Enrolled Plan: Research Concepts & Novelty Analysis
₹10,000.00 ₹25,000.00