This webinar will provide a comprehensive overview of the protocol development process with emphasis on tasks crucial to successful pathology evaluations in preclinical medical device studies.
In this webinar, the speaker will review the study-critical pathology operations at each phase of the process, including selection of endpoints and acceptance criteria, macroscopic tissue examination and collection strategies, histology processing and stain selection and histopathology scoring.
Attendees will also learn how ancillary imaging procedures, such as radiographic fracture analysis, micro computed tomography (microCT) and scanning electron microscopy (SEM), affect sample selection, tissue preservation and relate to histopathology evaluation.
The expert speaker will share recommended best practices for protocol development and pathology-driven tasks appropriate for medical device studies run under good laboratory practices (GLP), in accordance with ISO 10993-6 and in non-GLP environments.
Examples will be provided from a range of study types to illustrate strategies for selecting suitable controls, collecting appropriate tissues and designing applicable histopathology scoring. In addition, attendees will receive practical tips on avoiding common pitfalls that might compromise pathology success.
Register for this webinar today to learn how preclinical medical device studies can be optimized and how successful outcomes can be ensured for medical device research.
Keywords: Medical Device, Preclinical, CRO, Pathology, Diagnostics, Laboratory Technology, Medical Device Clinical Trials, Medical Device Development, Pre-Clinical