1 points | by peppernub 9 hours ago ago
1 comments
In regulated health software (EU MDR IIa), teams often need clinical alerting: thresholds, audit logs, patient prioritisation, etc.
Some teams build everything in-house, others integrate pre-certified components or platforms. From your experience:
When does building in-house make sense?
When does buying or integrating save real time (not just move work elsewhere)?
Any unexpected trade-offs?
Would love to hear real-world lessons, especially from teams shipping in 2024–2026.
In regulated health software (EU MDR IIa), teams often need clinical alerting: thresholds, audit logs, patient prioritisation, etc.
Some teams build everything in-house, others integrate pre-certified components or platforms. From your experience:
When does building in-house make sense?
When does buying or integrating save real time (not just move work elsewhere)?
Any unexpected trade-offs?
Would love to hear real-world lessons, especially from teams shipping in 2024–2026.