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5. Added value of drug-laboratory test interaction alerts in test result authorisation

6. ISO 15189 is a sufficient instrument to guarantee high-quality manufacture of laboratory developed tests for in-house-use conform requirements of the European In-Vitro-Diagnostics Regulation

9. EPMA-World Congress 2015: Bonn, Germany. 3-5 September 2015

11. Real-time monitoring of drug laboratory test interactions: a proof of concept

17. Clinical usefulness of drug-laboratory test interaction alerts: a multicentre survey

18. The end of the laboratory developed test as we know it? Recommendations from a national multidisciplinary taskforce of laboratory specialists on the interpretation of the IVDR and its complications

21. Real-time monitoring of drug laboratory test interactions: a proof of concept.

28. Diagnostic error as a result of drug-laboratory test interactions

29. Reflective testing - A randomized controlled trial in primary care patients.

30. The end of the laboratory developed test as we know it? Recommendations from a national multidisciplinary taskforce of laboratory specialists on the interpretation of the IVDR and its complications.

32. Global methodology for developmental neurotoxicity testing inhumans and animals early and chronically exposed to chemicalcontaminants

34. The use of error and uncertainty methods in the medical laboratory

36. Impact of interactions between drugs and laboratory test results on diagnostic test interpretation – a systematic review.

40. Opinion: redefining the role of the physician in laboratory medicine in the context of emerging technologies, personalised medicine and patient autonomy (‘4P medicine’)

42. Clinical impact of direct HDLc and LDLc method bias in hypertriglyceridemia. A simulation study of the EAS-EFLM Collaborative Project Group

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