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Global Site Contract Cycle Time
Expectations by Country
                     Most Used Global Countries
            Setting Appropriate Cycle Time Expectations
                 (Cycle Time Ranges in Total Days)
     0-45               46-90            91-120            121+
 ARGENTINA*          AUSTRALIA         AUSTRIA            FRANCE*
  BULGARIA           BELGIUM*           BRAZIL*            ITALY
     CHILE        CZECH REPUBLIC        CANADA             SPAIN
  COLOMBIA           GERMANY*           CHINA*
   HUNGARY            IRELAND          FINLAND
    INDIA*              JAPAN           GREECE
    ISRAEL           LITHUANIA         MALAYSIA
     PERU              MEXICO         PHILIPPINES
 PUERTO RICO       NETHERLANDS        SINGAPORE
   ROMANIA            POLAND*          S. KOREA
    SERBIA            RUSSIA*
  THAILAND            SWEDEN
   UKRAINE         SOUTH AFRICA
 US (CENTRAL)     UNITED KINGDOM
                     US (LOCAL)
Country Experience with Site
             Contracting
   Russia, Poland                                                Belgium
        Will accept CRO or sponsor template                           At least 3 agreements (Institution, Investigators,
        In Poland, need a final CTA before MOH submission              Pharmacy)
   Brazil                                                             Will use CRO or sponsor template but will need to
        Multi-party CTAs/back and forth                                modify for the 3 parties
        Access to drug an issue                                  France
   Argentina                                                          Prefers using own template
        CTAs usually not an issue                                     Investigator and Institution have separate
                                                                        agreements
        Costs are low
                                                                       No reference to US law or FDA regulations
   China
                                                                  Germany
        CTAS not an issue
                                                                       Accept no templates
        Costs are low
                                                                       Any new invention belongs to the investigator
        MOH rate limiting
                                                                  Latin America
   India
                                                                       Easy to negotiate
        Will accept CRO or sponsor template
                                                                       Chili and Peru have two party agreements (PI and
        2 party agreement (CRO and PI) – site does not sign            CRO)
        Costs are low                                                 Hospitals refuse to sign agreement
        Things move quickly                                           Clinical trial insurance not easy to obtain
                                                                       PIs don’t carry liability insurance

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Global Site Contract Cycle Time Expectations by Country

  • 1. Global Site Contract Cycle Time Expectations by Country Most Used Global Countries Setting Appropriate Cycle Time Expectations (Cycle Time Ranges in Total Days) 0-45 46-90 91-120 121+ ARGENTINA* AUSTRALIA AUSTRIA FRANCE* BULGARIA BELGIUM* BRAZIL* ITALY CHILE CZECH REPUBLIC CANADA SPAIN COLOMBIA GERMANY* CHINA* HUNGARY IRELAND FINLAND INDIA* JAPAN GREECE ISRAEL LITHUANIA MALAYSIA PERU MEXICO PHILIPPINES PUERTO RICO NETHERLANDS SINGAPORE ROMANIA POLAND* S. KOREA SERBIA RUSSIA* THAILAND SWEDEN UKRAINE SOUTH AFRICA US (CENTRAL) UNITED KINGDOM US (LOCAL)
  • 2. Country Experience with Site Contracting  Russia, Poland  Belgium  Will accept CRO or sponsor template  At least 3 agreements (Institution, Investigators,  In Poland, need a final CTA before MOH submission Pharmacy)  Brazil  Will use CRO or sponsor template but will need to  Multi-party CTAs/back and forth modify for the 3 parties  Access to drug an issue  France  Argentina  Prefers using own template  CTAs usually not an issue  Investigator and Institution have separate agreements  Costs are low  No reference to US law or FDA regulations  China  Germany  CTAS not an issue  Accept no templates  Costs are low  Any new invention belongs to the investigator  MOH rate limiting  Latin America  India  Easy to negotiate  Will accept CRO or sponsor template  Chili and Peru have two party agreements (PI and  2 party agreement (CRO and PI) – site does not sign CRO)  Costs are low  Hospitals refuse to sign agreement  Things move quickly  Clinical trial insurance not easy to obtain  PIs don’t carry liability insurance