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The qualification requirements encompass being a registered entity capable of supplying pharmaceutical products. Bidders must also submit relevant documentation that proves their operational capabilities and experience in executing similar contracts. Meeting these requirements increases the likelihood of successful bid submission.

Bidders are required to possess necessary certificates such as a valid registration with relevant healthcare authorities, quality assurance certifications (like ISO), and any pharmaceutical product-specific licenses. These documents must be submitted alongside the proposal to demonstrate compliance with regulatory requirements.

The registration process typically requires interested bidders to complete a registration form available on the government e-marketplace platform, along with uploading necessary documents including proof of experience and financial viability. Ensuring timely completion of this process is critical for eligibility.

Accepted document formats usually include PDF, DOCX, and Excel files. It is essential that bidders verify the guidelines prior to submission to avoid disqualification based on format discrepancies.

The evaluation and selection process involves a thorough review of submitted proposals based on technical and financial metrics. Evaluation panels typically assess compliance with all requirements, ensuring that selected bidders not only meet the minimum standards but also showcase the ability to deliver quality products efficiently.