Open Tender for 3083045 Borosil vacuum desiccators ID of 30mm,706201 NEST 35mm cell culture dishes with gripping ri

The eligibility requirements necessitate that suppliers be registered entities with provisions for MSE exemptions regarding experience criteria. Potential bidders must also demonstrate previous experience and provide relevant credentials.

Bid submissions must include essential certificates such as performance certificates, OEM authorization, and compliance documents as specified in the guide. Additional certification may be required to validate claims of exemptions.

To register, suppliers must complete the registration process online via the designated government platform. Documentation must include verification of company registration and compliance with the eligibility criteria.

Documents must adhere to the specified formats as mentioned in the tender instructions. Digital formats (PDF, DOCS, etc.) are generally accepted unless otherwise stated.

Yes, all consumables must meet the technical specifications and quality standards outlined in the tender document, ensuring they align with medical research requirements.

All supplied items must conform to established quality standards relevant for medical research. Details on specific standards utilize guidance from governing bodies as indicated in the documentation.

Compliance is critical, and bidders must ensure that all parts of their proposal align with regulatory standards for medical supplies and the specifications outlined in the tender.

Specific EMD conditions are defined within the tender document, ensuring financial commitment from bidders before the evaluation process begins.

Yes, successful bidders will be required to submit performance security as detailed in the tender documentation to guarantee fulfillment of contract obligations.

Payment terms are outlined in the tender and typically involve milestone payments. Further clarification can be obtained through the dedicated documents related to the tender.

The price evaluation will be based on total cost analysis and ability to provide compliant and quality consumables as specified in the BoQ.

Submissions will go through a group-wise evaluation process assessing technical criteria, compliance, and financial offerings, ensuring the selection of the most capable bidder.

The announcement of results will follow the evaluation period as outlined in the tender documentation, with notifications communicated through the official government platforms.

MSEs benefit from specific provisions like exemption from certain experience requirements, enabling increased participation opportunities in governmental procurements.

Startups are also encouraged to participate under the MSE provisions, with specific allowances aimed at fostering innovative suppliers in the medical research domain.

Yes, the tender is expected to align with the 'Make in India' initiative, promoting local sourcing and production where feasible, as guided by the central policies.

Specific local content provisions may apply, aiming to bolster indigenous suppliers and foster local industry growth within the medical research supply chain.