Human Biological Samples for Respiratory Research
Human Biological Samples Respiratory Viruses Research Focused Biobank
Biospecimens for Respiratory Research
hVIVO holds a unique collection of biospecimens collected under controlled conditions during Influenza A and RSV characterisation studies. Biospecimens are ethically approved, GCLP-processed, and accompanied by rich clinical metadata including PCR viral titres, antibody titres, symptom diaries, and donor demographics across multiple timepoints. Whether you need access to existing banked material or require a custom prospective collection designed around your study protocol, our team can support your requirements from initial scoping through to sample release.
Blood Products
Whole Blood
Serum
Plasma
PBMC
Buffy Coat
Swabs
Nasopharyngeal Swabs
Throat Swabs
Nasal Wick
Vaginal Swabs
Rectal Swabs
Additional Sample Types
Saliva
Urine
Tears
Hair
Nail
hVIVO operates in line with the Human Tissue Act 2004 and the HTA's Code of Practice E: Research across the full sample lifecycle, from collection and processing through to biobanking and release. Every sample is accompanied by traceable consent documentation, and our laboratory is GCLP-accredited (Good Clinical Laboratory Practice, RQA) to ensure quality assurance at every stage
Our Research Tissue Bank approval, granted under HTA Code of Practice E: Research, means samples can be used in ethically approved research projects without the need for a separate ethics application in most cases. If your project requires expanded scope or new prospective collections, our in-house medical writing team can support any additional regulatory or ethics submissions required, reducing the administrative burden on your team.
UK-Registered Research Tissue Bank
All samples are sourced through hVIVO's ethically approved Research Tissue Bank (IRAS ID 331455), with full consent, governance, and traceability built in from collection.
Longitudinal, Pathogen-Confirmed Samples
Samples collected across multiple timepoints from pre-infection to 28 days post-infection, with PCR-confirmed viral titres for Influenza A and RSV.
Custom Prospective Collection Available
hVIVO Biobank: Rich Clinical Context With Every Sample
Every sample in the hVIVO biobank is accompanied by detailed clinical metadata collected across multiple timepoints, from pre-infection through to 28 days post-infection. Metadata available with each sample set includes PCR-confirmed viral titres, serology and antibody titres, symptom scores and diary data, and full donor demographics. All participant data is managed by hVIVO's dedicated recruitment team in compliance with GDPR and UK Data Protection legislation, with no personally identifiable information shared with external parties.
Research Applications
Pre-clinical Drug
Discovery and Development Pathogen-confirmed longitudinal samples enable target identification and compound screening in physiologically relevant infectious disease models.
Diagnostics Developmen and Validation
Samples with confirmed viral titres and clinical metadata support the development and analytical validation of new diagnostic tests and screening tools.
Biomarker Discovery and Validation
Longitudinal biofluids from defined infection timepoints provide an ideal matrix for identifying and qualifying candidate biomarkers of disease progression and immune response.
Translational Medicine
Bridge the gap between preclinical findings and clinical relevance using samples from characterised human infection studies with full clinical context.
In Vitro Model Development
Primary cells and biofluids from well-characterised donors support the development and refinement of in vitro respiratory infection models.
Why Research Teams Choose hVIVO
- Unique Longitudinal Sample Sets: Pathogen-confirmed biofluids collected from pre-infection to 28 days post-infection for Influenza A and RSV. Depth and clinical context that off-the-shelf biobanks cannot match.
- GCLP-Accredited Processing: All samples are processed in our GCLP-accredited laboratory, ensuring quality, traceability, and regulatory acceptability for downstream research use.
- No Separate Ethics Application Needed: Our Research Tissue Bank approval covers most standard research uses. In most cases, your team can access samples without a separate ethics submission.
- Custom Prospective Collection: If our banked material does not meet your exact requirements, we can design and execute a new collection programme around your study design.
- Full Regulatory and Medical Writing Support: For projects requiring extended scope or new sample types, our in-house medical writing team can support any additional ethics or regulatory applications.
- End-to-End Sample Management: From collection and processing to long-term cryostorage and retrieval, all services sit under one quality system at our Greenwich facility.
Our ethical and regulatory review is built directly into how samples are collected, processed, stored, and released. All samples are sourced through an ethically approved UK Research Tissue Bank, ensuring consent, traceability, and governance are addressed upfront—reducing delays and risk for your research programme.