Common use of Study Data Clause in Contracts

Study Data. Institution and Investigator shall record and maintain complete medical records (including, without limitation, case report forms, laboratory work sheets and reports, and all relevant source documents) generated as a result of conducting the Study (collectively, the “Study Data”) in a timely, accurate, complete and legible manner in the form described in the Protocol. (a)

Appears in 2 contracts

Samples: Clinical Trial Agreement, smlouvy.gov.cz

AutoNDA by SimpleDocs

Study Data. (a) Study Data. Institution shall ensure that the Investigator keeps and Investigator shall record and maintain maintains complete medical records (including, without limitation, case report forms, laboratory work sheets and reports, and all relevant source documents) generated as a result of conducting the Study (collectively, the “Study Data”) in a timely, accurate, complete and legible manner in the form described in the Protocol. (a).

Appears in 2 contracts

Samples: Trial Agreement, Trial Agreement

AutoNDA by SimpleDocs

Study Data. Institution and Investigator shall record and maintain complete medical records (including, without limitation, case report forms, laboratory work sheets and reports, and all relevant source documents) generated as a result of conducting the Study (collectively, the “Study Data”) in a timely, accurate, complete and legible manner in the form described in the Protocol. Studijní data. Poskytovatel zdravotních služeb a Zkoušející budou zaznamenávat a udržovat kompletní lékařské záznamy (a)mimo jiné včetně formulářů pro záznamy o subjektech hodnocení, laboratorních záznamů a zpráv a všech příslušných zdrojových dokumentů) vytvořené v důsledku provádění Studie (dále společně označovány jako „Studijní data“) včas, přesně, úplně a čitelně podle právních předpisů ve formě popsané v Protokolu.

Appears in 1 contract

Samples: Clinical Trial Agreement Smlouva O Klinickém Hodnocení

Time is Money Join Law Insider Premium to draft better contracts faster.