Real-world-data & real-world-evidence platforms
Collecting health data in routine care to produce evidence that complements traditional trials — in China at pilot stage since the 2019 Boao Lecheng programme, where 15 medical product units had registered using real-world data by June 2024.
1 · What it gives
Real-world research collects data on patient health in real-world settings to generate evidence about the use and effects of medical products. Real-world evidence complements the limits of traditional clinical trials. In China it is at pilot stage: the Boao Lecheng pilot started in 2019 and, as of June 2024, 15 medical product units there had passed registration and listing using real-world data.
2 · What it replaces 6
3 · How to implement 4 steps
- 1Goals and feasibilitySet research goals and test feasibility.
- 2ProtocolDesign the study protocol.
- 3Data and governanceCollect data under governance.
- 4AnalysePerform statistical analysis and report the evidence.
4 · Who delivers
Matched suppliers (matched automatically)
| Avani | Indonesia | Producer | active |
| Accra Compost and Recycling Plant Limited | Ghana | Producer | active |
| BioTerra | Uruguay | Services / consulting | active |
| GEA Group | Germany | Distributor | active |
| Meihua Biological 梅花生物 (SSE 600873) | China | Research / RTO | active |
| FENRI Co., Ltd. | Taiwan | Not classified | active |
| Fermelanta | Japan | Producer | active |
| AGROSAVIA | Colombia | Research / RTO | active |
| ALBORS SRL | Animal Health & Welfare | Italy | Research / RTO | active |
| ATTO | Brazil | Distributor | active |
| Abolis Biotechnologies | France | Producer | active |
| Absolute | India | Not classified | active |
Leading companies and institutes (from the brief)
The Hainan Institute of Real-World Data and Peking University’s National Institute of Pharmaceutical and Medical Device Regulatory Science are named. Others are matched by the portal under Services.
5 · Rules & route to market
state registration ~10-15 working days after expert assessment; new substances need notification
Information, not legal advice — confirm the procedure for your product. (2026-10-06)
United States
The sources reviewed on 2026-10-16 identified no the US regulator or standard specific to this technology. Treat the route as case-by-case and ask for a check.
European Union
The sources reviewed on 2026-10-16 identified no the EU regulator or standard specific to this technology. Treat the route as case-by-case and ask for a check.
China
In China the NMPA governs the area through guidelines such as the Guiding Principle for Real-world Evidence to Support Drug Development and Review.
6 · Money: tenders & grants
| Grant | Health of ecosystems and wild species, predictions and impacts on human health, in the face of existing and … European Commission · EU | Sep 22, 2027 341 days |
| Grant | Additional activities for the European Partnership of Agriculture of Data European Commission · EU | Nov 26, 2026 41 days |
| Grant | DOD Defense Health Agency (DHA) Research & Development FY23-FY27 BROAD AGENCY ANNOUNCEMENT for Extramural … Defense Health Agency Contracting Activity - DHACA · United States | Sep 30, 2027 349 days |
| Grant | DoW Joint Warfighter Medical, Military Medical Research and Development Award Defense Health Agency Contracting Activity - DHACA · United States | Nov 16, 2026 31 days |
| Grant | First in Human and Early Stage Clinical Trials of Novel Investigational Drugs or Neuromodulatory Device-based … National Institutes of Health · United States | Oct 15, 2027 364 days |
7 · Tech stack & innovations
Main risks from the sources: limited data accessibility, data privacy, and data quality and standardisation.
Sources 5
- Amr.hainan.gov.cn — amr.hainan.gov.cn 2026-10-16
- Link.springer.com — link.springer.com 2026-10-16
- Pmc.ncbi.nlm.nih.gov — pmc.ncbi.nlm.nih.gov 2026-10-16
- Gov.cn — www.gov.cn 2026-10-16
- Doi.org — doi.org 2026-10-16