--- title: "Design resources" canonical: "https://research.refined.site/space/Research/108494912/Design%20resources" format: markdown --- ### [Statistics advice](https://clinicaldecisions.atlassian.net/wiki/spaces/Research/pages/48333346) The Research & Knowledge Centre is pleased to offer access to an in-house statistical service for those needing advice about the design and analysis of research, audit and evaluation activities. **Your project should already be registered with us to make use of this service**. Individual appointments can be arranged by emailing your protocol to [waitemataresearch@tewhatuora.govt.nz](mailto:waitemataresearch@tewhatuora.govt.nz) . We provide statistic advice on a range of topics including trial design, data collection and statistical software tools. Please click the [link ](https://clinicaldecisions.atlassian.net/wiki/spaces/Research/pages/48333346)to see the full list. ### [Qualitative research advice and resources](https://clinicaldecisions.atlassian.net/wiki/spaces/Research/pages/112689153) The Research & Knowledge Centre offers in-house support for qualitative research design and analysis, aiming to enhance practice-based research capacity and capability through qualitative research education and methodological assistance; for more information or to arrange a discussion, contact [waitemataresearch@tewhatuora.govt.nz](mailto:waitemataresearch@tewhatuora.govt.nz) ### [Researcher directory](https://clinicaldecisions.atlassian.net/wiki/spaces/Research/pages/112787481) Our Researcher Directory fosters connections among researchers from various health professions, serving as a source of inspiration and facilitating meaningful interactions between novices and established researchers with shared interests and methodologies. ### [Good clinical practice](https://clinicaldecisions.atlassian.net/wiki/spaces/Research/pages/112492591) The ICH E6 Good Clinical Practice (GCP) Guideline was finalised in 1996 describing the responsibilities and expectations of all participants in the conduct of clinical trials, including investigators, monitors, sponsors and IRBs. --- ###### Last reviewed November 2023 Page Coordinator: Judy Williamson