MedBrains
Software development and consulting firm (founded 2018) that designs information systems to collect, integrate, analyse and share medical and pharmaceutical data. Primary activities include implementation of pharmacovigilance and regulatory-data standards, automated medical-term recognition and coding via natural language processing (NLP), validation and conversion of regulatory safety-report formats, and delivery of web-based, API and self-hosted software for safety-data processing. The organisation has supported regional and national pharmacovigilance services and performed E2B R3 conversions for externally funded safety studies.
Industries
Nr. of Employees
small (1-50)
Products
Self-hosted medical-term auto-coding engine
Engine for automatic recognition and coding of medical terms in free text; supports multiple dictionaries and languages, available via API or as a self-hosted deployment.
Pharmacovigilance validation and conversion API (SaaS)
API and SaaS to manage and validate safety reports in E2B formats, including conversion between versions and transformation between XML and simplified JSON representations.
Queryable safety archive derived from product information
Queryable archive of therapeutic indications and adverse reactions extracted from product information and encoded to controlled terminology to support safety analysis and label harmonization.
Self-hosted medical-term auto-coding engine
Engine for automatic recognition and coding of medical terms in free text; supports multiple dictionaries and languages, available via API or as a self-hosted deployment.
Pharmacovigilance validation and conversion API (SaaS)
API and SaaS to manage and validate safety reports in E2B formats, including conversion between versions and transformation between XML and simplified JSON representations.
Queryable safety archive derived from product information
Queryable archive of therapeutic indications and adverse reactions extracted from product information and encoded to controlled terminology to support safety analysis and label harmonization.
Services
Ad-hoc data integration, ETL and conversion of datasets into regulatory formats (including E2B R3).
Cloud-hosted service and APIs for validation and conversion of safety reports between E2B versions and between XML and simplified JSON representations.
Development of bespoke web applications, APIs and backend systems for medical-pharmaceutical data using server-side frameworks and relational databases; offered as on-site, remote or managed services.
Ad-hoc data integration, ETL and conversion of datasets into regulatory formats (including E2B R3).
Cloud-hosted service and APIs for validation and conversion of safety reports between E2B versions and between XML and simplified JSON representations.
Development of bespoke web applications, APIs and backend systems for medical-pharmaceutical data using server-side frameworks and relational databases; offered as on-site, remote or managed services.
Expertise Areas
- Pharmacovigilance data management
- Regulatory data standards and reporting (E2B, IDMP, MedDRA, WHODrug)
- Medical NLP and automated terminology coding
- Data engineering and ETL pipeline development
Key Technologies
- E2B R2/R3 safety-report standards
- IDMP and controlled medicinal terminology standards
- MedDRA and WHODrug coding
- FAERS/VAERS and national reporting datasets
News & Updates
Performed conversion of study data to E2B R3 safety-report format for subsequent submission to a European safety database on behalf of an external research partner during the COVID-19 pandemic.
Performed conversion of study data to E2B R3 safety-report format for subsequent submission to a European safety database on behalf of an external research partner during the COVID-19 pandemic.