Contract manufacturing of a sterile, lyophilized cold kit for south african nuclear energy corporation (necsa)

• Ability to produce sterile, lyophilized or freeze‑dried pharmaceutical kits in accordance with gmp requirements. • Demonstrated gmp‑certified manufacturing facilities and relevant experience in sterile drug production. • Submission of the standard bid returnable documents (bid form, technical and financial proposals, compliance certificates) as specified in the tender pack. • Confirmation of the exact list, number of copies, signing and submission method for the returnable documents with the procuring entity. • Compliance with typical south african procurement requirements (e.g., Tax clearance, b‑bbee verification, CIDB registration, cipc registration, professional licences, local content) although specific items are not listed. • Ability to meet the project timeline and deliver the sterile kits within the stipulated schedule. • Provision of evidence of quality assurance systems and traceability for the manufactured kits.