Procurement Opportunity: Anti - AB Blood Grouping Reagent (V2),Anti - D Blood Grouping Reagent,Urine Test Strip,HBsAg Rapid in MORADABAD, UTTAR PRADESH

The eligibility requirements for bidders include being a registered entity with a minimum average annual turnover of ₹7 Lakhs over the last three years, and at least 3 years of experience in supplying similar medical products.

Bidders must submit documentation including experience criteria, past performance records, turnover statements, OEM authorization, and any additional documents specified in the ATC.

No, there is no exemption from the EMD requirement for this tender as the MSE and Startup provisions do not apply.

All products must comply with the Medical Device Rules (MDR) 2017 and hold an ISO:13485 certification. They must also have a sufficient shelf life from the date of manufacture.

The evaluation process follows a total value-wise method, initially assessing technical qualifications followed by a reverse auction for price determination among the qualified bidders.

A performance security is mandated at 3% of the total contract value, which is typically lodged post-award of the contract.

No MSE purchase preference is available as part of this tender, which applies equally to all bidders.

Bidders are required to upload their documents electronically through the GEM platform as per specified formats and guidelines.

Payment terms after successful delivery adhere to the conditions stipulated in the tender documents, which usually involve a direct transfer upon verification of supplied goods.

Successful bidders must ensure delivery of the medical products within 15 days of receiving the purchase order.

Yes, bidders will be notified regarding the evaluation results through the official GEM platform.

Bidders are encouraged to understand and comply with guidelines issued under the Make in India policy as part of their operational strategy.

Yes, bidders must provide documentation reflecting compliance with all applicable quality assurance standards as defined by the Medical Device Rules in India.

Bidders must complete a registration process on the GEM platform, detailing their credentials, product offerings, and compliance with specified regulations.

International bidders may need to check the specific eligibility criteria and compliance requirements applicable to foreign entities as outlined in the tender documentation.