Safety Reports. Institution and Investigator must record and report all serious AEs in accordance with the Protocol.
Appears in 5 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
Safety Reports. Institution and Investigator Investiga- tor must record and report all serious AEs in accordance with the Protocol.
Appears in 3 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
Safety Reports. Institution and Investigator must record and report all serious AEs in accordance with the Protocol.
Appears in 1 contract
Samples: Clinical Trial Agreement
Safety Reports. Institution and Investigator Provider must record and report all serious AEs in accordance with the Protocol.
Appears in 1 contract
Samples: Healthcare Agreement
Safety Reports. Institution and Investigator must record and report all serious AEs in accordance with the Protocol. nebo jiným Regulačním orgánům ve vztahu k průbehu Klinického hodnocení.
Appears in 1 contract
Samples: Clinical Study Agreement
Safety Reports. Institution and Investigator must record and report all serious AEs in accordance with the Protocol. „Data společnosti Idorsia“), která jsou úplná, aktuální, přesná, uspořádaná a čitelná: 2.
Appears in 1 contract
Samples: Clinical Trial Agreement
