Research Support
Research Protocol Development Service
Ensure your research study is scientifically sound, methodologically accurate, and ethically compliant with our Research Protocol Development Service. We provide comprehensive assistance in study design, methodology, sample size calculation, data collection tools, and ethics submission. Our team prepares clear, organized, and publication-ready research protocols that are fully aligned with institutional and regulatory standards.
Why Medics Research
A research protocol is essential for ensuring that a study is scientifically rigorous, ethically conducted, and methodologically consistent. It provides a clear roadmap for achieving your study objectives, minimizing bias, safeguarding participant rights, and facilitating ethics committee approval. A well-developed protocol also serves as an effective communication tool among researchers, guiding your study from planning to completion.
Our Services
Identify and define the research gap based on current scientific evidence and literature. Formulate clear and achievable research objectives aligned with the identified gap. Develop an appropriate study design, define inclusion/exclusion criteria, and establish a detailed methodology ensuring accuracy, reproducibility, and scientific validity.
Our Process
Our Workflow Process
Get real-time updates that keep you informed throughout every stage.
Help
Who We Help
Research design, data analysis, and manuscript preparation for academic publications and conferences.
Guidance in research methodology, data interpretation, and project report preparation.
Complete thesis and manuscript support, including study design, statistics, and manuscript development.
Advanced research guidance, statistical analysis, and publication assistance for high-impact journals.
Get professional assistance to develop a high-quality, compliant, and approval-ready research protocol.
Frequently Asked Questions
Everything you need to know about using Medics Research...
01
What is a research protocol?
A research protocol is a structured document that defines the study’s objectives, design, methodology, and statistical analysis plan. It serves as a roadmap for conducting research in a scientifically valid and ethically compliant manner.
02
How do you identify the research gap?
We conduct a detailed literature review using recent and relevant scientific publications to identify areas that lack sufficient evidence or where findings are inconclusive. This helps in formulating a focused research question.
03
How do you calculate the sample size, and what information is needed?
We calculate sample size using statistical formulas and software (G*Power, OpenEpi, nQuery) based on study type, expected effect size, confidence level, and power. Required information includes study objectives, outcome variables, expected differences, standard deviations or event rates, significance level (α), power (1–β), and study design.
04
Can you help with the Institutional Ethics Committee (IEC) or IRB submission?
Absolutely. We prepare all required documents — including protocol, informed consent forms, participant information sheets, and annexures — and provide guidance to address reviewer or ethics committee feedback.
05
How long does it take to develop a complete protocol?
The duration depends on the complexity of the study. Typically, protocol development (including literature review, design, and sample size calculation) takes 7 to 10 working days, depending on the amount of input and revisions required.