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GEM

Contract Bidding Open For item 1,item 2,item 3,item 4,item 5,item 6,item 7,item 8,item 9,item 10,item 11,item 12,item 13 in KHORDHA, ODISHA

Bid Publish Date

03-Jan-2025, 10:09 pm

Bid End Date

25-Jan-2025, 9:00 am

Progress

Issue03-Jan-2025, 10:09 pm
Technical01-Sep-2025, 5:04 pm
Financial
AwardCompleted
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Quantity

86

Category

item 1

Bid Type

Two Packet Bid

Categories 20

Public procurement opportunity for Indian Navy item 1, item 2, item 3, item 4, item 5, item 6, item 7, item 8, item 9, item 10, item 11, item 12, item 13 in KHORDHA, ODISHA. Quantity: 86 issued by. Submission Deadline: 25-01-2025 09: 00: 00. View full details and respond.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

item 1 , item 2 , item 3 , item 4 , item 5 , item 6 , item 7 , item 8 , item 9 , item 10 , item 11 , item 12 , item 13

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENTINDIAN NAVY

BID & GeM Expert Consultancy

End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.

Bid Preparation GeM Registration Document Filing

Free consultation · 24h response

Documents 4

GeM-Bidding-7332708.pdf

Main Document

BOQ Document

BOQ

BOQ Document

BOQ

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Bill of Quantities (BOQ) 13 Items Sign in for GEM prices

#1

item 1

Drape surgical disposable for eye surgery 5mtrx5mtr Specifications microembossed plastic. midsize 102cm X 122 cm, rectangular 13 cmm X10 cm adhesive incise area single fluid catch bag with lid tapes

10 pkt Delivery: 30 days
#2

item 2

Cotton ear buds 75 Stem/bot

5 bott Delivery: 30 days
#3

item 3

3 piece IOL 13.0mm length 3 piece, prolene haptics, 13.0mm length, 6.0mm, biconvex optic 10 degree angulation of haptic with A constant of 118.4, US FDA Approved

2 no Delivery: 30 days
#4

item 4

NYLON 10-0 non absorbable, monofilament, black, polyamide, spatulat ed neeble, 3/8 circle, double arm box of 12

1 box Delivery: 30 days
#5

item 5

Prefilled Syringe methylcellulose stenle with cannula for intraocular use. Must not contain any particulate matter and must be manufacture by company manufacturing US FDA drugs

20 pfs Delivery: 30 days
#6

item 6

Inj trypan blue 0.15% w/v Sterile 1ml vial in pack of 05. For cataract surgery

1 vial Delivery: 30 days
#7

item 7

Triamcinolone Acetionide 40 mg 1 ml suspension. box of 5 vials intraocular injection

1 bott Delivery: 30 days
#8

item 8

Proparacaine hydrocholoride eye drops USP 0.5% bottle of 5ml

10 bott Delivery: 30 days
#9

item 9

INTRACAMERAL MOXIFLOXACIN 0 5Mg in 01 ml Preservative free

10 pfs Delivery: 30 days
#10

item 10

Lignocaine 1% for intra-ocular use vial of 1 ml (preservative free)

10 no Delivery: 30 days
#11

item 11

Malayugin Ring disposable 6.25mm diameter which can be injected via 2.2 mm or larger incision and gives 8 points of fixation on the iris

1 no Delivery: 30 days
#12

item 12

Pilocarpine Intracameral Inj 0.5% Pilocarpine nitrate intra-ocular Inj without preservatives, amp of 01ml each Preservative free

5 amp Delivery: 30 days
#13

item 13

Disposible Bimannual Irrigation Aspiration cannula for cataract surgery

10 pair Delivery: 30 days

Required Documents

1

Experience Criteria

2

Past Performance

3

Bidder Turnover *In case any bidder is seeking exemption from Experience / Turnover Criteria

4

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

Technical Results

S.No Seller Item Date Status
1
SIGMA PHARMACEUTICALS   Under PMA
-09-01-2025 17:04:29

Financial Results

Rank Seller Price Item
L1
SIGMA PHARMACEUTICALS   Under PMA
Item Categories : item 1,item 2,item 3,item 4,item 5,item 6,item 7,item 8,item 9,item 10,item 11,item 12,item 13

Frequently Asked Questions

Key insights about ODISHA tender market

What are the eligibility requirements for participating in this procurement?

The eligibility requirements include being a registered entity, capable of demonstrating prior experience with similar procurement contracts, and meeting financial stability benchmarks as laid out in the tender document. Specifically, bidders may receive exemptions from experience requirements if they are classified as Micro, Small, and Medium Enterprises (MSEs) or startups, promoting a level access point for participation.

What certifications are required for the procurement of drugs and consumables?

Bidders must possess all relevant compliance certificates that conform to national healthcare standards. This includes certifications that validate the quality standards of the drugs and consumables they propose to supply. Additionally, bidders will require proof of registration with regulatory authorities governing pharmaceutical supplies.

How does the registration process work for this tender?

To participate in the tender, vendors need to be registered on the governing procurement portal. The registration process typically involves verifying the company’s legal standing and financial status along with submitting necessary documentation as outlined in the tender requirements. Access to the procurement portal can be obtained via their official website.

What formats are accepted for document submissions?

Documents must be submitted in the required digital formats specified within the tender documents. Generally, PDF format is often preferred for official documents to maintain integrity. Proper formats ensure that all uploaded information is compliant with submission criteria.

What are the technical specifications outlined in the procurement documents?

The technical specifications detail the necessary quality, efficacy, and safety standards all drugs and consumables must meet. These specifics include compliance with nationally recognized product standards and requirements for tracking and documentation throughout the supply chain.

Are there specific quality standards that must be adhered to?

Yes, all supplied drugs and consumables must adhere to established national and international quality standards for medical products. This includes compliance with regulations enforced by relevant health authorities, ensuring safety and efficacy.

What are the compliance requirements for bidders?

Bidders must comply with all specified quality regulations and must provide documentation that affirms their operational adherence to healthcare standards. This includes timely submission of compliance certificates and a commitment to quality management practices.

What criteria exist for testing the supplied products?

Testing criteria will be defined in the tender documents, assessing both pre-delivery and post-delivery quality measures. Bidders may be responsible for conducting quality tests ensuring every batch meets the necessary specifications prior to approval.

What are the details surrounding the Earnest Money Deposit (EMD)?

The Earnest Money Deposit (EMD) is generally a percentage of the bid price that demonstrates commitment and seriousness in the bidding process. Specific details regarding the EMD amount required can be found in the tender documents and must be submitted alongside the bidding proposal as proof of intent.

What are the performance security requirements set by the Department of Military Affairs?

Bidders may be required to furnish performance security as a safeguard against potential non-performance during the terms of the contract. This security can typically take the form of bank guarantees or performance bonds, which should be detailed in the contract agreements.

What are the payment terms for successful bidders?

Payment terms will be specified in the tender documentation, generally outlining payment schedules and conditions which may vary depending on whether it is milestone-based or upon full delivery. Ensuring clarity in these terms is crucial for compliance.

How will bids be evaluated and selected for this procurement?

Bids will be evaluated based on a total value-wise evaluation method, where financial proposals and adherence to technical specifications will be assessed comprehensively. The evaluation process may consider historical performance, financial stability, and overall compliance.

How will bidders be notified of the selection results?

Bidders will be informed through official communication from the issuing authority regarding the status of their submission. This typically includes detailed notifications via the procurement portal or directly to the contact provided during the registration.

What benefits do Micro, Small, and Medium Enterprises (MSEs) receive in this tender?

MSEs may benefit from exemptions on experience requirements, allowing newer companies to compete on a more level playing field. This initiative is designed to encourage smaller entities' participation in government procurement processes.

Are there provisions for startups within this procurement process?

Startups can take advantage of similar exemptions regarding experience in relation to MSEs. This supports innovative companies in entering the procurement space and facilitates a diverse supply chain which can lead to improved services and products.

How does this procurement align with the 'Make in India' policy?

The procurement process encourages local sourcing of products, thereby aligning with the 'Make in India' initiative aimed at promoting domestic manufacturing capabilities. Bidders focusing on local production will be given favorable consideration during the evaluation process.