ISO/IEC 17025. Preparation of buffers, reagents, and media necessary for sample processing in compliance with plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) activities. Responsible and supervise the preparation of media and reagents to use during sample processing and
1.1.4. Preparation of buffers, reagents, and media necessary for sample processing in compliance with plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) 2. Responsible and supervise the preparation of media and reagents to use during sample processing and
ISO/IEC 17025. Preparation of buffers, reagents, and media necessary for sample processing in compliance with plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) activities. Responsible and supervise the preparation of media and reagents to use during sample processing and
health facilities and communities for data study entry Provide regular updates on the study to key stakeholders
health facilities and communities for data study entry Provide regular updates on the study to key stakeholders
the quality control of patient files and data entries (i.e., eCRF's, CRF's) Support the storage and archiving
requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings
the quality control of patient files and data entries (i.e., eCRF's, CRF's) Support the storage and archiving
requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings
before the submission date. Ensure sufficient stock levels in order to perform scheduled analysis before testing required. Receive, label and pack stock away. Verify media prior to use according to laboratory procedures