Biobanking and Specimen Storage Management
Course overview
This course covers the systematic collection, storage and retrieval of biological specimens for research and diagnostic use. Delegates study cold chain management, inventory control and the ethical and consent considerations that govern stored samples. The programme supports facilities that maintain long term specimen collections.
What you will gain
- Establish collection and processing standards for specimens
- Manage cold chain and cryogenic storage conditions
- Operate inventory and tracking systems for stored samples
- Apply consent, ethics and access governance
- Plan for equipment failure and business continuity
- Maintain records that support sample traceability
Who should attend
- Biobank and repository staff
- Research laboratory managers
- Specimen storage and inventory technicians
- Quality and governance officers in research settings
Upcoming sessions
| Date | City | Duration | Fees | |
|---|---|---|---|---|
| 14 to 16 Dec 2026 | Durban | 3 Days | R13,000 | Book |
| 12 to 14 Apr 2027 | Pretoria | 3 Days | R13,000 | Book |
| 9 to 11 Aug 2027 | Cape Town | 3 Days | R13,000 | Book |
Fees are per delegate and exclude VAT. Dates run in the second week of each month. We also deliver this course on your own schedule, in-house or live online.
More in Laboratory & Microbiology
Laboratory Quality Management Systems and ISO/IEC 17025 Accreditation
This programme prepares laboratory managers and quality staff to build, document and maintain a management system that meets the requirements of ISO/IEC 17025. Participants examine competence, impartiality and consistent operation of testing and calibration laboratories, and learn how to prepare for a successful accreditation assessment. Practical sessions cover document control, corrective action and the transition from internal quality goals to formal recognition.
Laboratory Safety and Biosafety Management
This course equips laboratory personnel to identify, assess and control the physical, chemical and biological hazards found in a working laboratory. Delegates study biosafety levels, containment practices and the safe handling of infectious agents alongside general occupational safety duties. The training links regulatory expectations to day to day behaviour on the bench.
Good Laboratory Practice (GLP) for Regulated Studies
This programme explains the principles of Good Laboratory Practice as applied to non clinical health and environmental safety studies. Participants learn how GLP governs study conduct, data integrity, facilities and personnel responsibilities. The course helps laboratories align their practices with the expectations of regulatory bodies and monitoring authorities.