Engagement of Consultants to review, pilot-test and evaluate paper-based National Laboratory Information System (N-LIS) tools and specific disease program e-LIS
The National Medical Laboratory Services Policy (2021-2025) made a provision for the development of a National Laboratory information Management System. It states that; “there shall be improved data collection and laboratory information management system to facilitate good surveillance practices and timely response to epidemics and notifiable diseases. Similarly, it enjoined the government at all levels and relevant stakeholders to “establish a robust electronic Laboratory Information Management System that is linked to all the tiers of the laboratory.”
There is currently no National LIMS that collect laboratory data from all disease programmes. To address this situation, two consultants were engaged by the Federal Ministry of Health during the RSSH I in (add year) with the support from Global fund through Management Systems for Health to support the development of the National Laboratory Information Management Systems (NLIMS).
A national paper-based tool which can be converted to electronic tool have been developed for collecting and reporting laboratory data across program areas. This was developed through a robust collaborative process with inputs from country laboratory systems experts. FMOH (MLSD), NCDC, CHAI, FHI, CDC, NMEP, NTBLCP, NASCP, NLTWG and other key stakeholders. Consultants also led the development of Indicators to be tracked nationally. Data flow chart (from the facility to the National HMIS database), an SOP to guide the use of the paper and electronic tools as well as a system to ensure the quality of the data (paper based and electronic data) was also developed. It is expected that the tools developed will be piloted in 12 states after which evaluation will be done to finalize the National LIMS which will then be followed by scale-up in more facilities.
The use of Laboratory Information Management System (LIMS) is sub-optimal as most laboratory data collection and reporting tools are still paper-based. Each disease program has different LIMS, and data is not uniformly shared at the national level. Some laboratories, including stand-alone, have software that is not linked to HMIS.
There are major gaps in laboratory service delivery data availability and quality in Nigeria. The use of multiple reporting tools (paper-based) for the same disease program by different health facilities based on supporting implementing partners and the existence of parallel laboratory information systems for data collection/reporting across different disease program results in considerable potential for duplication, overlap, and confusion. There is, therefore, the need for a harmonized approach to laboratory data collection and reporting from the health facility level that will be linked to the national DHIS-2 platform.
To this end, NACA will engage two (2) Consultants to review, pilot-test and evaluate paper-based National Laboratory Information System (N-LIS) tools and specific disease program e-LIS
2. Goal and Objectives
· To conduct review/assessment of the draft N-LIS tools (paper-based)
· To develop protocol for pilot testing of N-LIS paper-based tools
· To lead the pilot testing of the draft N-LIS tools (paper-based) in 12 states
· To finalize the draft N-LIS paper-based tools using findings from the pilot testing
· To assess available disease programs e-LIS and provide recommendation for establishment of integrated national e-LIS
1. Scope of work
The scope of work and expected outputs/deliverables will be the following:
· Collect, review and analyze all the necessary documents to fully substantiate all stages of development of the National Laboratory Information System
· Collect, review and analyze all the necessary documents to fully understand the administrative framework for Laboratory Information Management Systems in Nigeria.
· Collect, review and analyze the international and national level approach for Laboratory Information Management System.
· Carry out stakeholder analysis to bring out the roles and responsibilities of key players and institutions that play a vital role in Laboratory Information System Management.
· Assessment, documentation and analysis of current LIMS tool
· Based on the processes mentioned above and in consultation with the Project Team, prepare a protocol for the pilot assessment of N-LIS draft tools.
· Based on the processes mentioned above and in consultation with the Project Team, prepare a comprehensive pilot assessment checklist and SOP for N-LIS
· Draft specific, detailed and practical steps for training and pilot testing paper-based tool in selected facilities (three facilities per 12 states for paper-based pilot
· Facilitate two working group consultations (organized by FMOH (MLSD)) and present the draft N-LIS pilot assessment results and revised N-LIS paper-based tool to the key stakeholders including NLTWG.
· Produce a well-written and detailed data analysis and report of the pilot testing of draft N-LIS tools.
· Produce a well-written and comprehensive report highlighting:
· Current responses by key stakeholders in Laboratory Information Management System use in various facilities in the country.
· Recommendations to strengthen linkages between organizations involved in the Laboratory Information Management System.
· Resource Directory of all the relevant Government Departments / Ministries / NGOs with focal points.
· A detailed presentation to be made by the consultant after the completion of the assessment tool on the salient features of the tool at a NLTWG meeting organized by FMOH (MLSD) and NACA.
2. Duration of Consultancy
The duration of the consultancy is Fifteen (15) days (10 days for actual work and 5 days for facilitating training)
3. Number of Consultants Required
Note: each consultant should only propose to provide services in 6 states
4. Required Qualification /Experience:
· A post-graduate or equivalent qualification/ degree in Medical Laboratory Science, Health Information Management, Laboratory Information Management System, Public Health, Health Programs Monitoring and Evaluation, Laboratory System Strengthening, Bioinformatics or any other relevant discipline.
· At least 5-7 years of prior work experience in dealing with health or specifically laboratory monitoring and evaluation interventions especially in the regional and international context.
· Demonstrated knowledge and experience in undertaking research especially in the area of Laboratory Information System.
· Demonstrated experiences and skills in facilitating stakeholder/working group consultations.
· Familiarity with Nigeria Lab Information System and NLIS including facility flow
· Relevant regional and international experience will be an added advantage.
The project seeks to identify experts that fulfill the above criteria and have demonstrated ability of involving key stakeholders (Ministries, Departments, Agencies, civil society etc.) to provide relevant expertise and bring a wider perspective in developing the assessment tool.
7.`COLLECTION OF REQUESTS FOR PROPOSAL (RFP) DOCUMENT
The Request for Proposal (RFP) can be downloaded from this link; https://www.naca.gov.ng/wp-content/uploads/2021/12/2021.11-RFP-LIMS-Consulatnts.pdf
8. GUIDELINE FOR SUBMISSION AND OPENING OF DOCUMENTS
The detailed Proposal must be in English Language and submitted in three (3) hard copies each (one original & two copies) of the requested documents and proposal. The documents shall then be enclosed and sealed in one (1) single outer envelope, and clearly marked at the topmost right corner “LIMS Consultant” and the Name, Address, Email and Phone Number of the Consultant boldly written at the back of the envelope, with acknowledgement to NACA office at the address below. Alternatively, Submission can be made to pro[email protected].
a. Deadline for Submission: The deadline for the submission of proposal should not be later than Thursday 12 noon of 8th April, 2022. The submission(s) received will be opened immediately after closing at NACA Conference Room in the presence of consultants that choose to attend.
9. ADDRESS FOR INFORMATION AND SUBMISSION OF PROPOSALS
National Agency for the Control of AIDS (NACA)
Ground Floor Room 1.08
No. 3 Zinguinchor Street, Beside AEDC Office, Wuse zone 4, Abuja
Email: [email protected]
Tel: +234-9-4613726-9 Fax: +234 94613700
10. GLOBAL FUND CODE OF CONDUCT
You shall get acquainted with the global fund code of conduct for suppliers using this link below: https://www.theglobalfund.org/media/3275/corporate_codeofconductforsuppliers_policy_en.pdf
Accepting this invitation shall serve as an acknowledgement and agreement to abide by the Global Fund Code of Conduct for Suppliers.
· Late submissions will not be accepted.
· NACA shall verify any or all documents and claims made by applicants and will disqualify consultants with falsified documents and claims.
· If it is determined that submitted documents and claims have been falsified, the consultant may face prosecution in a court of Law.
· NACA shall not be held responsible for any disqualified proposal as a result of any omission or deletion relating to the submission guidelines.
· This advertisement shall not be construe a contract to any Consultant, nor shall it entitle any Consultant submitting documents to claim any indemnity from NACA.
· NACA is not bound to shortlist any Consultant, and reserves the right to annul the bidding process at any time without incurring any liabilities or providing reason.