Common Contracts
4 similar Clinical Trial Research Agreement contracts
Clinical Trial Research Agreement New Zealand Association of Clinical Research (NZACRes) - Collaborative or Cooperative Research Group (CRG)Clinical Trial Research Agreement • March 23rd, 2021
This Agreement is to be used where; a Collaborative or Cooperative Research Group acts as, and assumes all of the agreed responsibilities of a Sponsor, as defined by the current Committee for Proprietary Medicinal Products (CPMP)/International Conference on Harmonisation (ICH) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95); and the approved Ethics Committee is satisfied that the Study will not be carried out principally for the benefit of the Manufacturer or distributor of the Investigational Product in question. See the Guidance Document for additional information. The body of this Agreement (that is from the following page to the execution clauses) is intended to be identical to the standard form, a copy of which is located at www.nzacres.org.nz. Any textual change to the body of this Agreement is to be ignored, and referenced instead to the standard form, as amended by Schedule 5 by way of Special Conditions. Where there is conflict between the main body of th
Clinical Trial Research Agreement New Zealand Association of Clinical Research (NZACRes) - Collaborative or Cooperative Research Group (CRG)Clinical Trial Research Agreement • March 23rd, 2021
This Agreement is to be used where; a Collaborative or Cooperative Research Group acts as, and assumes all of the agreed responsibilities of a Sponsor, as defined by the current Committee for Proprietary Medicinal Products (CPMP)/International Conference on Harmonisation (ICH) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95); and the approved Ethics Committee is satisfied that the Study will not be carried out principally for the benefit of the Manufacturer or distributor of the Investigational Product in question. See the Guidance Document for additional information. The body of this Agreement (that is from the following page to the execution clauses) is intended to be identical to the standard form, a copy of which is located at www.nzacres.org.nz. Any textual change to the body of this Agreement is to be ignored, and referenced instead to the standard form, as amended by Schedule 5 by way of Special Conditions. Where there is conflict between the main body of th
Clinical Trial Research Agreement New Zealand Association of Clinical Research (NZACRes) - Collaborative or Cooperative Research Group (CRG)Clinical Trial Research Agreement • June 26th, 2018
This Agreement is to be used where; a Collaborative or Cooperative Research Group acts as, and assumes all of the agreed responsibilities of a Sponsor, as defined by the current Committee for Proprietary Medicinal Products (CPMP)/International Conference on Harmonisation (ICH) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95); and the approved Ethics Committee is satisfied that the Study will not be carried out principally for the benefit of the Manufacturer or distributor of the Investigational Product in question. See the Guidance Document for additional information. The body of this Agreement (that is from the following page to the execution clauses) is intended to be identical to the standard form, a copy of which is located at www.nzacres.org.nz. Any textual change to the body of this Agreement is to be ignored, and referenced instead to the standard form, as amended by Schedule 5 by way of Special Conditions. Where there is conflict between the main body of th
Clinical Trial Research Agreement New Zealand Association of Clinical Research (NZACRes) - Collaborative or Cooperative Research Group (CRG)Clinical Trial Research Agreement • March 5th, 2017
This Agreement is to be used where; a Collaborative or Cooperative Research Group acts as, and assumes all of the agreed responsibilities of a Sponsor, as defined by the current Committee for Proprietary Medicinal Products (CPMP)/International Conference on Harmonisation (ICH) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95); and the approved Ethics Committee is satisfied that the Study will not be carried out principally for the benefit of the Manufacturer or distributor of the Investigational Product in question. See the Guidance Document for additional information. The body of this Agreement (that is from the following page to the execution clauses) is intended to be identical to the standard form, a copy of which is located at www.nzacres.org.nz. Any textual change to the body of this Agreement is to be ignored, and referenced instead to the standard form, as amended by Schedule 5 by way of Special Conditions. Where there is conflict between the main body of th
