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Invitation to Bid - Tab Rivaroxaban 20mg,Bosentan 62.5 mg tab,N Butyl cyanoacrylate 0.5ml Inj,Tobramycin 300 mcg respul in PANCHKULA, HARYANA

Bid Publish Date

03-Jan-2025, 10:04 am

Bid End Date

24-Jan-2025, 11:00 am

EMD

₹8,315

Progress

Issue03-Jan-2025, 10:04 am
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

24824

Categories 9

Public procurement opportunity for Indian Army Tab Rivaroxaban 20mg, Bosentan 62. 5 mg tab, N Butyl cyanoacrylate 0. 5ml Inj, Tobramycin 300 mcg respules, MDI spacer with mask and fish mouth valve for pediatrics set, GLYCOPYRENIUM RESPULE, SPACER WITH ZEROSTAT TECHNOLOGY, BUDESONIDE 320 MCG plus FORMETEROL 9 MCG MULTI UNIT DOSE INHALER, Tab Selexipag 200 mg, Lignocaine 15per 10per topical nasal spray, Nicotine chewing gum2 mg, Nicotine chewing gum4 mg, STERITALC F4, Benzonatate 100 mg Tab, Ambroxyl 15mg plus terbutaline 1. 25plus guaiphensin 50 mg per 5 mi, Cough lozenges dextromethorphan, Montelukast sodium 10 mg tab plus fexofenadine 180 mg, Glutaraldeyde 2per aqueous soln with activator 5 liter, Tab Acebrophyline 100mg, Mesna 200mg Inj, Inj zoster vaccine recombinat adjuvanted in PANCHKULA, HARYANA. Quantity: 24824 issued by. Submission Deadline: 24-01-2025 11: 00: 00. View full details and respond.

Documents 4

GeM-Bidding-7283272.pdf

Main Document

View File

Referenced Document

Buyer uploaded ATC document Click here to view the file .

Referenced Document

attached categories, trials are allowed as per approved procurement policy of the buyer nodal Ministries)

Referenced Document

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Required Documents

1

Experience Criteria

2

Past Performance

3

Bidder Turnover

4

Certificate (Requested in ATC)

5

OEM Authorization Certificate

6

OEM Annual Turnover

7

Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria

8

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

Frequently Asked Questions

Key insights about HARYANA tender market

## FAQs
What are the eligibility requirements for participating in the RESP DRUGS tender?

The eligibility requirements include being a registered entity, possessing prior experience in supplying pharmaceutical products, and meeting specific turnover criteria. Additionally, bidders must provide necessary documentation to support their claims for exemptions if requested.

What certificates are required for the RESP DRUGS tender?

Bidders must submit certifications reflecting their compliance with technical specifications, an OEM Authorization Certificate, and proof of past performance related to similar pharmaceutical supplies. Any additional supporting documentation requested must also be included.

How can I register to bid for the RESP DRUGS tender?

The registration process requires bidders to sign up on the official tender platform, submit relevant business information, and comply with the necessary verification checks as detailed in the documentation.

What document formats are accepted for the RESP DRUGS tender submission?

Accepted document formats include PDF and DOC. Bidders should ensure that all submitted certifications and compliance documents adhere to these formats to avoid disqualification.

What are the technical specifications for the drugs included in the RESP DRUGS tender?

The technical specifications require that all drugs meet safety and efficacy standards as outlined in the BoQ. Detail in compliance certificates must reflect alignment with specifications for Rivaroxaban, Bosentan, N-Butyl cyanoacrylate, and other medications listed.

What quality standards must bidding companies adhere to?

Bidders must comply with international quality standards pertaining to pharmaceuticals, ensuring that all items meet established health regulations and guidelines prior to delivery.

What are the compliance requirements for the RESP DRUGS tender?

Compliance requirements include adherence to all listed specifications, submission of required documents, and demonstration of quality assurance processes that meet industry standards.

What testing criteria apply for the RESP DRUGS tender submissions?

Submissions must undergo evaluation that includes testing for quality and safety of the pharmaceuticals offered. This may involve third-party validation or inspection as deemed necessary by the department.

What details should I know about the Earnest Money Deposit (EMD)?

The EMD required for this tender is ₹8315. This amount ensures the bid's seriousness and is returned after the evaluation, subject to compliance with tender conditions.

Are there performance security requirements after winning the tender?

Yes, successful bidders will be required to provide performance security to ensure fulfillment of contract obligations, as outlined in the tender documentation.

What are the payment terms associated with the RESP DRUGS tender?

Payment terms will be specified in the contract after award, typically involving a payment schedule tied to delivery milestones and acceptance of goods.

How will the evaluation and selection process be conducted?

The evaluation and selection process will be item-wise based, focusing on compliance with submission requirements, technical specifications, pricing competitiveness, and overall past performance.

How will bidders be notified of the results of the RESP DRUGS tender?

Bidders will be notified of the results through the tender platform or via official communication channels as defined in the tender documentation upon conclusion of the evaluation process.

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

MSEs have preferential consideration during the evaluation process, allowing them to compete effectively and potentially enjoy relaxed eligibility criteria for certain aspects of the tender requirements.

Are there specific provisions for startups in this tender?

Yes, startups may benefit from easier qualification criteria and consideration of their unique capabilities in the context of this tender.

Does the RESP DRUGS tender require compliance with 'Make in India' policies?

Yes, bidders are encouraged to ensure their submissions contribute to the 'Make in India' initiative, focusing on local procurement and manufacturing processes whenever possible.

What are the local content and procurement rules applicable to this tender?

Bidders must adhere to local content requirements as per relevant procurement policies that promote the use of domestically sourced materials and services in their bids.