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Resources

Find documents and tools that support every stage of clinical research at the Platform. From protocol templates to training materials and SOPs, these resources are designed to help you plan, manage, and deliver high-quality clinical trials.

Study Planning & Protocol Development – Templates and tools to help you design and prepare your study Protocol template_5June2025.docx

 

Clinical SOPs

MULCLPQ 2: Unit SOP for Obtaining Informed Consent.

LSHTM 9: Clinical Trials Set Up Guidance

MULCLPQ 3: Unit SOP on Clinical Safety Reporting.

MULCLPQ 4: SOP on Managing Medical Emergencies

MULCLPQ 6: SOP for verifying volunteer/ participants eligibility

MULCLPQ 5: SOP for Medical Referral

MCP 004: HIV Counselling

Pharmacy SOPs

MULPPPQ 7: Use and Maintenance of Pharmacy Equipment SOP

MULPPPQ 8: Use and maintenance of Biosafety Cabinet or Laminar Flow Hood SOP

MULPPPQ 9: Transfer of IP from Unit Pharmacy for off-site administration SOP

MULPPPQ 11: Cleaning and Pest Control SOP

MULPPPQ 13: Temperature Monitoring for Concomitant Medicines and Ancillary Supplies

MULPPPQ 6: SOP for Emergency transfer of investigational products.

MULPPPQ 2: Storage of investigational products SOP

MULPPPQ 10: SOP on Expiry Date Extension and Re-labelling of Investigational Products

MULPPPQ 5: SOP for Accountability and Disposal of Investigational Products.

MULPPPQ 4: SOP for prescribing and dispensing Investigational Products and Concomitant Medication 
MULPPPQ 3: SOP on temperature and humidity monitoring of stored Investigational Products

MULPPPQ 1: SOP on Importation and receipt of study products.

MULPPPQ 3.2: Appendix 2 Eltek alarm notification test log

MULPPPQ 3.3: Appendix 3 Manual temperature and humidity monitoring log

MULPPPQ 6.3: Appendix 3 Checklist for Emergency Transfer of Investigational Product to a Back-Up Unit located in same room

MULPPPQ012.1: MULPPPQ012 _Appendix_1_Stock_Card

MULPPPQ 7.1: Appendix 1 Problem Assessment-Corrective action log

MULPPPQ 7.2: Appendix 2 Schedule of maintenance template

MULPPPQ 9.1: Appendix 1 IP Transfer form

MULPPPQ 3.1: Appendix 1 Alarm rota template

MULPPPQ 6.2: Appendix 2 Checklist for Emergency Transfer of IP stored at room temperature (15 to 25o C) to a Back-Up Storage room

MULPPPQ 6.1: Appendix 1Checklist for Emergency Transfer of Investigational Product to a Back-Up Unit

MULPPPQ 7.3: Appendix 3 Equipment maintenance log

MULPPPQ 3.3: Appendix 3 Manual temperature and humidity monitoring log

Newsletters

IMPALA
IMPALA newsletter Issue 4
IMPALA newsletter Issue 3
IMPALA newsletter issue 2
IMPALA newsletter Issue 1

MOBILE MEN
MOBILE MEN Newsletter July 2025
MOBILE MEN Newsletter Oct 2024
MOBILE MEN Newsletter May 2024
MOBILE MEN Newsletter October 2023

If you’re not sure what you’re looking for or need something specific, get in touch with us at [email protected]

About Us

For more than three decades the MRC/UVRI I &  LSHTM  Uganda  Research  Unit has generated evidence that underpins national, regional, and global responses to HIV and other pressing public‑health challenges. The Clinical Research and Trials Platform is the next step in that legacy: a central hub for designing, delivering and overseeing high-quality clinical trials. 

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Our Services

From concept to close-out, our Clinical Research and Trials Platform provides comprehensive support to help research teams deliver high-quality, impactful studies. We work closely with investigators, sponsors, and regulatory authorities to ensure every trial is scientifically robust, ethically compliant, and operationally efficient.

Publications

Our publications cover a broad spectrum of research, from clinical trials and observational studies to implementation science and social science, sharing evidence that informs health policy and practice

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Knowledge Transfer & Exchange (KTE) is the Platform’s bridge between science and real‑world impact. We enable KTE by working with investigators to ensure research findings are effectively communicated to policy makers, practitioners, communities, and other stakeholders.