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The eligibility requirements include being a registered entity, providing relevant documentation such as past performance records, and certifications that validate compliance with industry standards. Bidders must demonstrate their capability through operational history in supplying pharmaceutical products.

Yes, bidders must submit various certificates, including OEM authorization certificates, quality assurance certificates, and any other documentation as specified in the tender's technical section. Additionally, any claiming exemption from standard experience criteria must provide supporting documents.

The registration process for bidders typically involves creating an account on the relevant GEM portal, filling in required details, and submitting necessary documents for verification. After documents and eligibility have been validated, bidders can access and submit their bids accordingly.

Documents must be submitted in specified formats, primarily PDF and DOC. It is crucial to adhere to the detail-oriented submission formats mandated in the tender guidelines to ensure compliance and facilitate smooth processing.

The payment terms will typically be determined post-evaluation but generally require successful bidders to invoice once their goods are delivered and accepted as per the specifications. Compliance with EMD and performance security requirements is critical to finalize payment arrangements.

This comprehensive approach ensures all essential information is conveyed correctly, supporting the engagement of quality providers while facilitating clarity in the tendering process.