Bid Publish Date
14-Jan-2025, 4:03 pm
Bid End Date
24-Jan-2025, 5:00 pm
Value
₹20,00,000
Location
Progress
Directorate Of Medical Education And Research invites bids for Fully Automated Coagulation Analyzer (V2) (Q2) in MUMBAI, MAHARASHTRA. Quantity: 1. Submission Deadline: 24-01-2025 17: 00: 00. Submit your proposal before the deadline.
Quantity
1
Bid Type
Two Packet Bid
Bid Validity
30 (Days)
Bid Type
Service
Evaluation
Total value wise evaluation
Inspection Required
No
Tech Clarification Time
2 Days
Min. Avg. Annual Turnover
10
OEM Avg. Turnover
10
Past Performance
10 %
Experience Required
3 Year (s)
Arbitration Clause
No
Mediation Clause
No
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
No
Item Category
Fully Automated Coagulation Analyzer (V2) (Q2)
End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.
Free consultation · 24h response
Main Document
GEM_CATEGORY_SPECIFICATION
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
Experience Criteria
Past Performance
Bidder Turnover
Certificate (Requested in ATC)
OEM Authorization Certificate
OEM Annual Turnover
Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria
the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer
Key insights about MAHARASHTRA tender market
The eligibility requirements include being a registered entity, demonstrating a minimum average annual turnover of 10 Lakh, having three years of past experience in supplying similar medical equipment, and meeting all specified technical requirements.
Bidders must include certificates proving compliance with quality standards, OEM authorization documents, and evidence supporting past performance and turnover. Proper certification is crucial to validate eligibility for this tender.
Registration for this tender typically involves filling out the required forms as outlined in the tender documents. Bidders must ensure they meet the eligibility criteria before proceeding with registration.
The documented submissions must typically be in PDF format, as these are commonly required for official bids. Review the specific instructions in the main document to verify the exact formats acceptable.
The technical specifications include capabilities for various coagulation tests, adherence to quality manufacturing standards, and the provision of comprehensive operational support. Detailed specifications can be found in the tender documentation.
Yes, bidders must comply with recognized quality standards in medical equipment manufacturing. These standards are designed to ensure that the equipment provided meets safety and efficacy requirements in a clinical setting.
Compliance requirements include meeting technical specifications, providing necessary documentation of turnover, and obtaining certifications as outlined. Failure to meet these could result in disqualification.
The tender outlines that the products must undergo testing to ensure they meet all technical and operational benchmarks before acceptance. Testing procedures need to follow established medical device regulations.
While the exact EMD amount is not specified, it is a common requirement to secure bid submissions. Participants should refer directly to the tender documents for precise details on EMD.
Post-award, bidders must submit a performance security that ensures adherence to the contract terms. The amount and form of the required performance security will be outlined in the tender documentation.
Payment terms typically follow completion and acceptance of delivered equipment, contingent on providing required documentation and may include milestone payments as outlined in the bid specifications.
Price evaluation will consider the total cost proposed by bidders along with compliance with technical specifications and past performance history to ensure a holistic selection process.
Bids can generally be submitted electronically through the tender portal, following the electronic submission guidelines provided in the main document.
While specific dates are not provided in this description, bidders should reference the main tender document to stay informed regarding submission timelines and related deadlines.
The evaluation process will assess all submitted bids based on technical compliance, financial offering, and provider capacity, using a rubric based on total value-wise evaluation criteria.
Yes, all bidders will be notified about the outcome of their submission following the conclusion of the evaluation process. Regular communication will be maintained throughout the tender lifecycle.
MSEs may benefit from exemptions regarding specific eligibility criteria, allowing them greater access and opportunity to participate in tenders like this one, fostering inclusivity in public procurement.
Startups are encouraged to apply, with special provisions available to facilitate their participation, promoting innovation and fostering a competitive market.
The tender aligns with the 'Make in India' initiative by promoting domestic manufacturing and encouraging local suppliers to engage in the bidding process, reinforcing local economic development.
Yes, bidders are expected to comply with local procurement rules, including stipulations about sourcing and production that promote local industry engagement in the supply of medical technologies.