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Showing below up to 100 results in range #1 to #100.
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- (hist) Challenges [86 bytes]
- (hist) 4 Continuous improvement [157 bytes]
- (hist) 1.4.3.4 Academia-academia: Research as collaboration [168 bytes]
- (hist) 1.4.2.7 Animal care and use [248 bytes]
- (hist) 1.4.2.8 Human data protection [254 bytes]
- (hist) 1.4.2.1 Biosafety [290 bytes]
- (hist) Dossier [305 bytes]
- (hist) 1.4.2.3 Radioactivity [313 bytes]
- (hist) Risk Management Case Studies [337 bytes]
- (hist) 1.5.3.2 Facilities [376 bytes]
- (hist) 1.5.2.2 Management [394 bytes]
- (hist) 1.5.3.1 Personnel [398 bytes]
- (hist) 1.5.3.6 Documentation requirement for sample and material [404 bytes]
- (hist) 1.5.3.4 Electronic information system [424 bytes]
- (hist) 1.5.3.3 Laboratory and experimental equipment used for measurement [433 bytes]
- (hist) Why quality matters [436 bytes]
- (hist) 1.5.3.5 Organization-specific know how [456 bytes]
- (hist) 4.3.2.3 Revising NEEDs [478 bytes]
- (hist) 1.5.4.1 Independence of internal compliance assessment [481 bytes]
- (hist) 1.5.3 Management of resources [524 bytes]
- (hist) 3.2.4 Training on specific methods, tasks and activities [544 bytes]
- (hist) 1.5.2.1 Organigram [577 bytes]
- (hist) 1.5.2 Roles and responsibilities of involved personnel and organization [626 bytes]
- (hist) 3.2.2 Good Research Practice training [627 bytes]
- (hist) 1.4.2.5 Risks to unborn life [635 bytes]
- (hist) 1.4.1 Research ethics [641 bytes]
- (hist) 4.3.2.4 Deleting NEEDs [652 bytes]
- (hist) 1.5.3.7 Retained personnel records [660 bytes]
- (hist) 1.5.2.6 Supporting team [664 bytes]
- (hist) 1.5.2.7 Quality professionals [665 bytes]
- (hist) 1.5.4.2 Internal assessment of the organizations' quality professionals [681 bytes]
- (hist) 1.4.2.6 Handling of controlled substances [683 bytes]
- (hist) 1.4.2.2 Chemical safety [750 bytes]
- (hist) Abbreviations [767 bytes]
- (hist) 1.4.2.4 Genetically modified organisms [769 bytes]
- (hist) 4.3.1.3 Revising items [782 bytes]
- (hist) Hauptseite [784 bytes]
- (hist) 1.5.2.5 Research team [882 bytes]
- (hist) Experimental Record [890 bytes]
- (hist) 4.3.1.2 Deleting items [898 bytes]
- (hist) 1.5.1 Quality policy [948 bytes]
- (hist) Examples for Errors [1,005 bytes]
- (hist) Information on the calculation of the priority ranking [1,053 bytes]
- (hist) 1.3.3 Promotion criteria within a research unit [1,170 bytes]
- (hist) 1.5.2.4 Principal investigators and study directors [1,192 bytes]
- (hist) 4.3.2 Using the EQIPD applications [1,267 bytes]
- (hist) Spot checks [1,352 bytes]
- (hist) 3.5.1 Animal and non-animal method and assay qualification [1,407 bytes]
- (hist) 1.5.5 Sustainability [1,421 bytes]
- (hist) 4.1.3 External Assessment [1,450 bytes]
- (hist) 3.2.1 General guidance on training [1,459 bytes]
- (hist) 1.3.1 Transparency [1,464 bytes]
- (hist) 3 Support Processes [1,470 bytes]
- (hist) 3.4.1 Animal characteristics, care and use [1,492 bytes]
- (hist) 2.1.10 Plausibility check [1,587 bytes]
- (hist) EQIPD [1,747 bytes]
- (hist) EQIPD Quality System [1,825 bytes]
- (hist) 3.4.1.6 Sanitation procedure [1,826 bytes]
- (hist) 3.4.1.9 Veterinary interventions during the study [1,829 bytes]
- (hist) 4.2.1 Installation of solutions, actions and mitigation strategies [1,880 bytes]
- (hist) 1.3.2 Sources of pressure and bias-producing communication of pressure [1,908 bytes]
- (hist) 1.4.3.1 Industry-academia: Research as service [1,990 bytes]
- (hist) 3.3.1 Fit-for-purpose working environment [2,071 bytes]
- (hist) 2.4.1 Non-public reporting [2,081 bytes]
- (hist) 1.4.2 Adherence to legal and regulatory considerations [2,156 bytes]
- (hist) 3.1.2.2 Process for witnessing of records [2,180 bytes]
- (hist) 4.3.1.1 Adding new items [2,184 bytes]
- (hist) 4.2.4 Key performance indicators [2,186 bytes]
- (hist) 2.2.3 Documentation of the experiment and deviations [2,195 bytes]
- (hist) 3.1.2.2 Process for witnessing of records [2,213 bytes]
- (hist) 2.1.2 Unique study ID [2,220 bytes]
- (hist) 1.3.4 Performance criteria and assessment [2,225 bytes]
- (hist) 2.4 Reporting [2,244 bytes]
- (hist) 2.3.1.1 Converting non-electronic information into an electronic form [2,307 bytes]
- (hist) 1.4.3.5 Expectations from public funders [2,378 bytes]
- (hist) 2.2.2 Use of template for (manual) data recording [2,391 bytes]
- (hist) 2.2.1 Use of SOPs for standard experiments [2,439 bytes]
- (hist) 4.1.3 External assessment [2,449 bytes]
- (hist) 3.4.1.11 Animal euthanasia procedures [2,452 bytes]
- (hist) 3.4.1.10 Surgical procedures [2,478 bytes]
- (hist) 1.5.4 Prevention of Conflict of Interest [2,535 bytes]
- (hist) Internal assessment [2,557 bytes]
- (hist) 3.4.1.4 Animal environmental conditions [2,584 bytes]
- (hist) 1.5.2.3 Process owner [2,604 bytes]
- (hist) 3.4.1.5 Food, watering and bedding [2,611 bytes]
- (hist) 1.4.3.2 Quality in collaborative research [2,647 bytes]
- (hist) 3.3.3 Management of research materials and reagents [2,681 bytes]
- (hist) 1.4.3 Quality in collaborative research [2,696 bytes]
- (hist) 2.3.2 Primary analysis and evaluation of raw data [2,773 bytes]
- (hist) 3.4.1.2 Animal procurement & identification [2,783 bytes]
- (hist) 3.1.3 Data security [2,883 bytes]
- (hist) 3.1.1 Platform to record data [2,895 bytes]
- (hist) 1.3.5 Reward system and incentives [2,903 bytes]
- (hist) EQIPD principles [2,911 bytes]
- (hist) 3.5.2 Protocols for methods and assays [3,018 bytes]
- (hist) 2.1.8 Randomisation [3,101 bytes]
- (hist) 4.3.2.2 Creating NEEDs [3,199 bytes]
- (hist) 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use [3,264 bytes]
- (hist) ARRIVE Essential - Results [3,322 bytes]
- (hist) 3.4.2.2 Antibody validation [3,323 bytes]
