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The eligibility requirements include being a registered entity, possessing authorized licenses for pharmaceuticals, and maintaining valid GST registration. To qualify, bidders must demonstrate relevant experience in supplying similar medicines and comply with all regulatory health standards.

Bidders must provide various required certificates such as company registration documents, valid GST certificates, and proof of compliance with Good Manufacturing Practices (GMP). Any additional certifications that ensure high-quality manufacturing standards will be beneficial during the evaluation.

The registration process typically involves completing required documentation as part of the tender submission. Interested parties should ensure they have their entity details, relevant licenses, and financial proposals prepared to ensure a smooth registration.

All submissions should preferably be conducted in PDF format to maintain integrity during the review process. This ensures that all documents remain unaltered and can be easily reviewed by the evaluation committee.

MSEs may benefit from relaxed eligibility criteria, increased evaluation support, and potentially favorable price evaluation considerations. This is in alignment with governmental policy initiatives to bolster local businesses and encourage their participation in public tenders.