Retrospective data studies
Approved analysis of existing laboratory and clinical records from partner sites.
I lead the Medbit Research Network, connecting universities, biotech teams and CROs in Australia, the UK and the USA with ethically governed study sites, laboratory support and clean, analysis-ready data in Bangladesh.
One point of contact between your study and the sites that run it.
Australia first, then the UK and USAI have run the bench, managed the lab and now coordinate the business, so I understand a study from sample tube to signed report.
PCR and molecular diagnostics through COVID-19, haematology and biochemistry QC, and field blood collection with a strict cold chain for the national STEPS survey.
As COO I run project coordination, partner relationships and quality processes, the same work your study depends on to start and finish on time.
I'm completing a Master of Medical Biotechnology at UTS and publish on haematology, antimicrobial resistance and genetic screening in Bangladesh.
Start with one well-scoped project. Every study runs under the approvals and consent pathway it needs.
Approved analysis of existing laboratory and clinical records from partner sites.
Participant recruitment and new data collection under an approved protocol.
Blood, serum and plasma collection, processing, coding and storage through qualified sites.
CRF and eCRF design, cleaning, coding, QC and analysis-ready datasets.
Literature searches, evidence extraction and protocol background research.
Tables, figures, posters, presentations and research reports.
How pricing works: you pay for research services, such as study setup, per-participant procedures, lab processing, data management and project management. We never sell patient data or samples.
You get one project owner, a clear scope, and a weekly or fortnightly update on recruitment, data quality, issues and next steps.
A discovery call about your question, and an NDA if needed.
We check which partner sites can realistically deliver it.
Scope of work, milestones, timeline and quotation.
Ethics and site approvals are in place before anything starts.
Trained staff, SOPs and data systems ready at each site.
Recruitment, data capture or sample collection as approved.
Quality checks, cleaning and coding as the data comes in.
Final QA, your dataset or report, and a documented close-out.
Ethics and governance come first in every project. That protects participants, and it protects the value of your data.
Leading operations and the Medbit Research Network.
COVID-19 PCR, molecular, haematology and biochemistry testing.
Lab operations, quality control and equipment calibration.
Field blood collection for the national STEPS survey.
Master of Medical BiotechnologyUniversity of Technology Sydney, 2024 to 2026
Bachelor of BiochemistryPrimeasia University, 2021
Co-authored studies from Bangladeshi hospitals and labs, the kind of work the network is built to support.
Archives of Clinical and Biomedical Research
Archives of Microbiology & Immunology
Journal of Radiology and Clinical Imaging
Molecular Mechanism Research, first author
Asian Journal of Biochemistry, Genetics and Molecular Biology
Teams that need flexible research capacity without setting up their own sites in South Asia.
The easiest way to test the network is a small, well-scoped pilot study or retrospective data project. If it works, we scale it up or move to a monthly research-support arrangement.
Tell me about your research question, population and timeline. I'll reply with a first view on feasibility, usually within two working days.