Progress
Quantity
1
N/a invites bids for Automated tissue processor (Q3) in RANCHI, JHARKHAND. Quantity: 1. Submission Deadline: 27-01-2025 17: 00: 00. Submit your proposal before the deadline.
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
No
Item Category
Automated tissue processor (Q3)
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Main Document
Referenced Document
Discover companies most likely to bid on this tender
Experience Criteria
Past Performance
Bidder Turnover
Certificate (Requested in ATC)
OEM Authorization Certificate
OEM Annual Turnover
Additional Doc 1 (Requested in ATC) *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
Extended Deadline
27-Jan-2025, 5:00 pm
Opening Date
27-Jan-2025, 5:30 pm
Extended Deadline
17-Jan-2025, 12:00 pm
Opening Date
17-Jan-2025, 12:30 pm
Key insights about JHARKHAND tender market
The eligibility requirements include being a registered entity with valid operational licenses, having a minimum average annual turnover of ₹20 Lakh for the last three financial years, and at least three years of relevant experience supplying similar equipment. MSE applicants may be exempt from certain criteria, provided they meet all technical specifications.
Yes, participants must submit various required certificates including the OEM authorization certificate, proof of experience criteria, past performance evidence, and bidder turnover validations as outlined within the bid documentation.
The registration process involves registering on the GeM portal, ensuring compliance with eligibility criteria, and submitting relevant documents as stated in the tender guidelines.
All submitted documentation should be in PDF format. Supporting financial documents, certificates, and technical specifications should reflect accuracy and conform to the conditions of the tender.
The technical specifications for the automated tissue processor include parameters such as 12 selectable programs, eight reagent stations, and a necessity for vacuum control. The device must also have essential components like an HDMI touch screen and the capability to integrate with laboratory workflows efficiently.
The equipment must comply with relevant quality standards, including but not limited to those required by the Drugs and Cosmetics Act, to guarantee safety and efficacy in medical applications.
Bidders must comply with all specified conditions in the bid document, including providing required certificates and adhering to quality specifications. Failure to meet any criteria may lead to disqualification.
Yes, the equipment will require validation against specified performance metrics as outlined in the tender document regarding operational efficiency and durability.
An EMD of ₹40,000 is required with the bid submission. Bidders seeking an exemption must provide valid support documents per the established guidelines on the GeM portal.
While performance security is not explicitly mandated in this tender, bidders should ensure they provide comprehensive service and warranty agreements reflecting the equipment's reliability.
Payments will typically be based on successful delivery and compliance with set conditions, including satisfactory installation and commissioning of the equipment.
Bids will undergo evaluation based on total value with an emphasis on past performance in delivering similar equipment. Documentation supplied will play a crucial role in determining compliance and overall qualifications.
Typically, bidders will receive notification via the GeM portal once the evaluation process is complete and results are finalized.
MSEs benefit from exemptions regarding experience and turnover requirements as long as the quality and technical specifications are met.
Startups do not have any exemptions concerning finances or experience as per the tender conditions, but they are encouraged to participate fully through alternative support channels where applicable.
The purchase of locally manufactured equipment aligns with 'Make in India' initiatives, as preference may be given to entities that comply with these guidelines in demonstrating local sourcing and production.
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Main Document
Referenced Document