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Bids are Invited For Brimonidine Tartrate + Timolol Maleate Drops (V2)

Bid Publish Date

14-Nov-2024, 11:31 am

Bid End Date

25-Nov-2024, 12:00 pm

Latest Corrigendum Available

Progress

Issue14-Nov-2024, 11:31 am
Corrigendum28-Nov-2024
AwardPending
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Quantity

600

Categories 1

The issuing authority announces a tender for Brimonidine Tartrate + Timolol Maleate Drops (V2). Quantity: 600. Submission Deadline: 25-11-2024 12: 00: 00. Last date to apply is approaching fast!

Documents 4

GeM-Bidding-7137677.pdf

Main Document

GeM Category Specification

GEM_CATEGORY_SPECIFICATION

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Corrigendum Updates

1 Update
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Update

28-Nov-2024

Extended Deadline

07-Dec-2024, 9:00 am

Opening Date

07-Dec-2024, 9:30 am

Frequently Asked Questions

What are the eligibility requirements for Brimonidine Tartrate + Timolol Maleate Drops?

The eligibility requirements include being a registered pharmaceutical supplier, demonstrating experiences in supplying similar products to government entities, and possessing all necessary certifications to comply with pharmaceutical regulations.

What certificates are required to participate in the bidding process?

Bidders must provide certifications that confirm adherence to all relevant compliance requirements and governmental standards specific to pharmaceutical products, including quality assurance certifications.

What is the registration process for bidders?

To participate in the bidding, suppliers must first register on the GEM portal. Following registration, they must upload all required documents, including certifications, product specifications, and financial statements to complete their profile for bidding.

Which document formats are accepted for submission?

Submissions must be made in common document formats such as PDF or Word. It is critical to ensure that all documentation complies with the expected formats specified in the submittal guidelines.

What are the technical specifications for the products being tendered?

The technical specifications for the products include detailed formulation requirements, potency levels, packaging specifications, and adherence to industry standards as clearly defined in the tender documentation.

What quality standards must the products meet?

All products must adhere to industry-recognized quality standards and fulfill regulatory compliance as stated by the relevant pharmaceutical authorities.

What are the compliance requirements for bidders?

Bidders must meet a range of compliance requirements, which include possessing necessary certifications and adhering to local regulations regarding pharmaceutical supplies.

Are there specific testing criteria for the products?

Yes, the testing criteria include ensuring that all products pass quality control and confirm consistency with the product specifications stipulated by the Department of Military Affairs.

What is the Earnest Money Deposit (EMD) requirement for this tender?

Bidders may be required to submit an Earnest Money Deposit as specified in the tender documents. The amount will typically depend on the total value of the bid and must be submitted along with the tender.

What are the performance security requirements post-award?

After the successful bid, the winning bidder must provide a performance security that guarantees contract fulfillment. Specifics regarding this requirement can be found in the tender document.

How are payment terms structured for the awarded contracts?

Payment terms will be detailed in the contract agreement, generally requiring certain milestones to be met before payments are made for products delivered.

What considerations are taken into account for price evaluation?

The price evaluation considerations will include the overall cost of the bid submission, quality of the offered product, and adherence to the technical specifications laid out within the documents.

How can bidders submit their proposals?

Bidders can submit their proposals electronically via the GEM portal, adhering strictly to the submission guidelines outlined in the tender documents to ensure their proposals are considered.

What are key timelines and deadlines for bidding?

Key timelines and deadlines for submission can be reviewed in the tender documentation. It is imperative that bidders adhere to these timelines to avoid disqualification.

How will bidders be notified of the results of their submissions?

Notifications regarding the results of submissions will be communicated through the GEM portal, and bidders are encouraged to check back for updates and further instructions.

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

MSEs may receive benefits such as relaxed qualification criteria and preferential pricing evaluations to promote inclusion and support to smaller businesses in the pharmaceutical sector.

Are there special provisions for startups in this tender?

Yes, startups are encouraged to apply, with specific provisions in place to facilitate their participation in the bidding process. These may include eased requirements and tailored evaluation processes.

How does this tender align with 'Make in India' policies?

Bidders must comply with the Make in India norms that promote local manufacturing and procurement. Preference will be given to products with significant local content as part of the evaluation criteria.

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