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The eligibility requirements include being a registered entity capable of supplying pharmaceuticals. Bidders must provide necessary documentation to support their eligibility, including relevant accreditation and proof of previous supplies in accordance with regulatory standards.

Bidders are required to submit quality certifications and compliance documents relevant to pharmaceutical standards. This includes manufacturing licenses and certifications proving adherence to Good Manufacturing Practices (GMP).

To participate in the tender, entities must register on the designated e-procurement portal. It involves filling out the necessary forms and submitting required documentation to establish legitimacy and capability.

Submissions must be made in electronic formats as specified in the tender documents. Generally, PDF is the preferred format, and all documents must be legible and organized as per the submission guidelines.

The technical specifications must align with the formulations detailed in the tender. Bidders should provide elements such as ingredient composition, dosage, and any other specific requirements outlined in the Bill of Quantities.

Yes, compliant production and supply of medications must adhere to both national and international quality standards, including certifications for quality assurance and pharmacological standards.

Bidders must comply with various regulatory requirements, including procurement policy adherence and ensuring the quality of the products supplied. All documents validating compliance must be submitted during the bidding process.

Further details regarding the Earnest Money Deposit will be specified in the tender documents. Bidders are required to submit EMD as part of their bid to ensure commitment during the tendering process.

The winning bidder must submit a performance security equal to a certain percentage of the contract value. This is to ensure fulfillment of the contract terms and quality assurance of the products supplied.

Payment terms will be specified in detail within the tender documentation. Typically, payments may be made upon successful delivery and acceptance of the pharmaceuticals as per contract conditions.

The evaluation of prices will be based on the overall cost-effectiveness of the bids while considering compliance with technical specifications. Competitive pricing combined with adherence to quality is a deciding factor.

Bids must be submitted electronically using the designated tender submission portal as specified in the tender documents. Ensure all required documents are included and formatted correctly before submission.

Key timelines, including the opening and closing dates for submissions, will be provided in the tender documents. Bidders should ensure their submissions are completed before the specified deadlines.

Results will be communicated through the e-procurement portal where the tender is hosted. Bidders are encouraged to check the portal regularly for updates regarding outcomes and further instructions.

MSEs may benefit from relaxed eligibility criteria and potentially preferred pricing evaluation to enhance competition. These provisions are aimed at fostering inclusive participation.

Yes, startups may avail themselves of special mandates that encourage their participation, including ease of eligibility conditions. Startups should refer to the tender documents for detailed provisions applicable to them.

Participating bidders must comply with any additional requirements as stated in the tender documents that align with 'Make in India' initiatives, promoting local manufacturing and sourcing of products.