MDR-TB Clinical Trials Capacity Building
TREAT TB builds capacity in supply chain management for MDR-TB clinical trials
Last month, TREAT TB hosted the second webinar in its series aimed at strengthening capacity to conduct high-quality clinical trials for multidrug-resistant tuberculosis (MDR-TB). This webinar focused on issues relating to supply chain management for MDR-TB trials and featured a presentation from Dr. Jan Komrska, senior pharmacist at Vital Strategies, followed by a question and answer session.
The discussion addressed the need for multiple supply chains to be designed, implemented, and managed in order to ensure the provision of the substantial resources required for clinical trials.
Dr. Jan Komrska also detailed key components to a successful supply chain, explaining that supply chain management requires dedicated and trained staff who are an integral part of the research team. It is important that they understand the needs of the customers, suppliers, and partners in order to ensure responsive supply chain design and management and reduce misunderstandings and errors.
The presentation also highlighted the importance of team work and good communication, including the use of clear, simple instructions, visual aids and logs.
TREAT TB’s MDR-TB clinical trial capacity building webinar series will continue over the coming months, with webinars scheduled for November, January, March, and May. Future topics to be addressed include regulatory requirements, institutional review boards and ethics approval, laboratory strengthening and community engagement, among others.
To listen to the latest webinar, please click here
To view Dr. Komrska’s presentation, see here
To read more about the TREAT TB project, click here.
¹ Horsburgh CR, Rusen ID, Mitnick CD. Optimizing MDR-TB clinical trials: insights from the first global MDR-TB Clinical Trials Landscape Meeting. Int J Tuberc Lung Dis. 2016; 20(12):1–3. doi: 10.5588/ijtld.16.0568
10 July, 2018
28th September, 2018
Challenges with MDR-TB Clinical Trial Implementation –
Sponsor and Site Perspectives. To view the slides and listen to the webinar, click here
Supply Chain Management for MDR-TB clinical trials
Regulatory Requirements, Institutional Review Boards and Ethics Approval
Please visit the page regularly for information on future webinars in the series and to access recordings from past webinars.