Information request for portable health technologies and poct devices for telemedicine

Primary RFI contact (submission): Elmie Engelbrecht, email: [email protected].

Enquiries: Dr Busisiwe Ndlovu, email: [email protected].

• Returnable Documents: (no specific list provided in the extract).
• Response format: single PDF document.
• Submission method: email the PDF to [email protected].
• Email subject line must read: "RFI 01/2025-26 Response: [Company Name] – PHT AND/OR POCT Devices".
• Submissions must be received no later than 30 January 2026 at 16:00 (4 pm).
• Late submissions will be rejected.
• No other submission forms or hard‑copy copies are mentioned.

• Objective: map the current market of Portable Health Technologies (PHTD) and Point‑of‑Care Testing (POCT) devices not covered by existing contracts.
• Scope: all devices usable at Primary Health Care (PHC) facilities across South Africa.
• Required information per device:

• Device/Product name and manufacturer.
• Intended use / analytes (e.g., HbA1c, HIV viral load, creatinine).
• Disease area/category.
• Sample type (finger‑prick, venous, urine, etc.).
• Time to result.
• Regulatory status (SAHPRA registration number, CE mark, FDA approval, etc.).
• Connectivity (Bluetooth/USB/Wi‑Fi) and data‑management software compatibility with SA systems (e.g., TIER.Net).
• Power and environmental requirements, training needs.
• Service and support model in South Africa (turn‑around time, local language support).

• Additional requirements: scalability, lead times for city vs rural clinics, supply‑chain capacity for all nine provinces, cost per test and device, warranty, post‑warranty terms, quality‑assurance and proficiency‑testing programmes, local correlation studies.

Provide the following information:

Part A – Company Profile:

• Company name and address.
• B‑BBEE status and certificate.
• Primary contact person, email and phone number.
• Confirmation of an established presence/support network in South Africa (yes/no with details).

Part B – Device Information (repeat for each device):

• Device/product name and manufacturer.
• Intended use / analytes.
• Disease area/category.
• Sample type.
• Time to result.
• Regulatory status (SAHPRA registration number, CE/FDA etc.).
• Connectivity and data‑management details (Bluetooth/USB/Wi‑Fi, compatibility with TIER.Net, printing capability).
• Operational requirements (power, temperature, humidity, training time).
• Service and support model (maintenance, turnaround time, local language support).

Part C – Scalability, Cost and Implementation:

• Lead time for delivery and consumable restocking (urban vs rural).
• Capacity to scale supply to all nine provinces.
• Cost per test (including consumables) and device cost; any bulk‑purchase discounts.
• Warranty period and post‑warranty support terms.
• Quality‑assurance procedures and proficiency‑testing programme.
• Evidence of local correlation studies.