Case Report Form or CRF definition

Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on each Study Subject (defined below).
Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on Ve Smlouvě jsou použity následující smluvní definice: Protokol: klinický protokol, na který je odkázáno výše, a který může podléhat čas od času změnám provedeným Zadavatelem (ve smyslu níže uvedené definice). Formuláře pro záznamy o subjektech hodnocení (Case Report Form) nebo CRF: formulář pro záznamy o subjektech hodnocení (v listinné či elektronické podobě) bude používán Místem provádění each Study Subject. klinického hodnocení za účelem záznamu veškerých informací požadovaných Protokolem, které podléhají oznamování Zadavateli ve vztahu ke každému Subjektu studie.
Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be Protokol: protokol klinického skúšania, na ktorý sa odvoláva táto zmluva a ktorý môže zadávateľ (definovaný nižšie) priebežne meniť a dopĺňať dodatkami. Pacientsky záznamový hárok (Case Report Form, „CRF”): pacientsky záznamový hárok (papierový alebo elektronický), ktorý má reported to Sponsor on each Study Subject (defined below). pracovisko skúšania používať na zaznamenávanie všetkých protokolom požadovaných informácií, ktoré sa majú hlásiť zadávateľovi o každom subjekte skúšania (definovanom nižšie). Study: the clinical trial that is to be performed in accordance with this Agreement and the Protocol for purposes of gathering information about the compound/medical device identified in the Protocol. S kúšanie: klinické skúšanie, ktoré sa má vykonať podľa tejto zmluvy a protokolu, s cieľom získať informácie o chemickej zlúčenine alebo zdravotníckej pomôcke, uvedenej v protokole.

Examples of Case Report Form or CRF in a sentence

  • The Institution and the Investigator shall record all data on a form provided by or on behalf of Biogen (Case Report Form or CRF).

  • Case Report Form or CRF: case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on each Study Subject (defined below).

  • Case Report Form or CRF: case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on each Study Subject.

  • Case Report Form or CRF: case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor or CRO on each Study Subject.

  • Significant amounts of consumed parent drugs and/or their active metabolites are discharged into domestic wastewater through urine or faeces (Zuccato and Castiglioni, 2009).

  • The Institution shall, and shall cause the Investigator to record all data on a form provided by or on behalf of Biogen (Case Report Form or CRF).

  • Case Report Form or CRF: case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on each Formuláře pro záznamy o Subjektech studie (Case Report Form) nebo CRF: formulář pro záznamy o Subjektech studie (v listinné či elektronické podobě) bude používán Místem provádění klinického hodnocení za účelem Study Subject.

  • The InstitutionFoundation shall, and shall cause the Investigator to, record all data on a form provided by or on behalf of Biogen (Case Report Form or CRF).

  • Case Report Form or CRF: case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to GSK on each Study Subject.

  • The Institution and the Investigator shall record all data on a form provided by or on behalf of Biogen Idec (Case Report Form or CRF).


More Definitions of Case Report Form or CRF

Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to GSK on each Study Subject. Study: the clinical trial that is to be performed in accordance with this Agreement and the Protocol for purposes of gathering information about the compound identified in the Protocol.
Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on each Study Subject. Study: the clinical trial that is to be performed in accordance with this Ve Smlouvě jsou použity následující smluvní definice: Protokol: klinický protokol, na který je odkázáno výše, a který může podléhat čas od času změnám provedeným Zadavatelem (ve smyslu níže uvedené definice). Formuláře pro záznamy o Subjektech studie (Case Report Form) nebo CRF: formulář pro záznamy o Subjektech studie (v listinné či elektronické podobě) bude používán Místem provádění klinického hodnocení za účelem záznamu veškerých informací požadovaných Protokolem, které podléhají oznamování Zadavateli ve vztahu ke každému Subjektu studie (ve smyslu níže uvedené definice). Studie: klinické hodnocení, které bude provedeno v souladu s touto Smlouvou Agreement and the Protocol for purposes of gathering information about the compound/medical device identified in the Protocol. a Protokolem pro účely získání a shromáždění informací o složce/zdravotnickém prostředku popsaném v Protokolu.
Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on Ve Smlouvě jsou použity následující smluvní definice: Smlouva: tato smlouva, včetně ustanovení o platbách a rozpočtu obsažených v Příloze A, jakož i v jakékoli jiné příloze k této smlouvě. Protokol: protokol o klinickém hodnocení nazvaný „ALXN1210-AHUS-311“, který může podléhat čas od času změnám provedeným Zadavatelem (ve smyslu níže uvedené definice). Formuláře pro záznamy o subjektech hodnocení (Case Report Form) nebo CRF: formulář pro záznamy o subjektech hodnocení (v listinné či elektronické podobě) each Study Subject. bude používán Místem provádění klinického hodnocení za účelem záznamu veškerých informací požadovaných Protokolem, které podléhají oznamování Zadavateli ve vztahu ke každému Subjektu studie (ve smyslu níže uvedené definice).
Case Report Form or CRF case report form (paper or electronic) to be used by Site to record all of the Protocol-required information to be reported to Sponsor on each Study Subject. Study: the clinical trial that is to be performed in accordance with this Agreement and the Protocol for purposes of gathering information about the compound identified in the Protocol. Study Subject: subject of the clinical trial within the meaning of Art. 51 (2) (g) of Act No. 378/2007 Coll., in other words an individual who participates in the Study, either as a recipient of the Investigational Product (defined below) or as a control.

Related to Case Report Form or CRF

  • ESDM Report means the Emission Summary and Dispersion Modelling Report prepared in accordance with the Procedure Document by Pinchin Environmental Ltd. and dated June 5, 2008 submitted in support of the application, and includes any amendments to the ESDM Report listed in Schedule A and all up-dated ESDM Reports prepared as required by the Documentation Requirements conditions of this Certificate.

  • Progress Report means the report similar in form and content to that attached hereto as Appendix III.

  • Project Report means a summary statement of the likely environmental effects of a proposed development referred to in section 58;

  • Acoustic Assessment Report means the report, prepared in accordance with Publication NPC-233 and Appendix A of the Basic Comprehensive User Guide,by HGC Engineering and dated August 22, 2008 submitted in support of the application, that documents all sources of noise emissions and Noise Control Measures present at the Facility and includes all up-dated Acoustic Assessment Reports as required by the Documentation Requirements conditions of this Certificate to demonstrate continued compliance with the Performance Limits following the implementation of any Modification.

  • Root Cause Analysis Report means a report addressing a problem or non-conformance, in order to get to the ‘root cause’ of the problem, which thereby assists in correcting or eliminating the cause, and prevent the problem from recurring.

  • Incident Report means a written report of any injury, accident, acts of physical aggression, or unusual incident involving an individual.

  • Settlement Report a report summarizing Revolver Loans and participations in LC Obligations outstanding as of a given settlement date, allocated to Lenders on a Pro Rata basis in accordance with their Revolver Commitments.

  • License Certificate means evidence of a license provided by Licensor to Licensee in electronic or printed form.