Bidder has to submit financial statements certified by an independent auditor as required in ITB Clause 15.2(a) for the period specified

Bidder has to submit other documents proofing its financial standing, as required in the BDS and in accordance with ITB Clause 15.2(b);

The average annual turnover for the period ———– does not exceed the amount of the financial proposal of the Bid in value specified in the BDS. 

Bidder has to complete the Delivery and Completion Schedule through Electronic Government procurement System as per template in Section 6, Statement of Requirements.

Bidder has to submit a Certificate of Pharmaceutical Product as recommended by the WHO for each item offered in accordance with ITB Clause 17.6

Having been submitted valid trade license or business organization registration certificate issued by the country of establishment in accordance with ITB Clause 4.6.(c)

A Bidder shall not have a conflict of interest. All Bidders found to have a conflict of interest shall be disqualified.

 Domestic Bidder has to submit VAT registration certificate issued by the tax authority (in case of contract value specified in BDS Clause 4.6(b)(ii), in accordance with ITB Clause 4. 6(b)(ii).

The Bidder has to submit the Form Data on Joint Ventures, the Agreement governing the formation of joint venture, or letter of intent to form JV (ITB 36.2(J))

 Domestic Bidder has to submit a valid tax clearance certificate issued by the tax authority, in accordance with ITB Clause 4.6(b)(iii); 

Bidder have nationality in accordance with ITB Sub-Clause 4.2; 

Bidder has to submit relevant professional practice certificates, Clause 4.6(b)(iv);

Bidder has to provide in the Bidder Certification of Compliance

Form information related to its professional qualification and capability for the period specified in the BDS Clause 14.1; and ITB 36.3(b)

Bidder has to submit List of pharmaceuticals being manufactured by the Bidder with product registration/license number and date in accordance with ITB Clause 17.6; 

Bidder has to submit Certificate from the competent Regulatory

Authority (RA) that the manufacturer is licensed to manufacture the

Pharmaceutical and Medical Equipment offered in accordance with ITB

Clause 17.4 (only Bidders who are not primary manufacturers).

Bidder has to submit Descriptive technical literature

Bidder has to provide in the Bidder Certification of Compliance Form information about major relevant contracts successfully completed in the number and period

Bidder has to provide the Statement attesting the origin of the Pharmaceutical and Medical Equipment and Related Services offered

Bidder has to submit Good Distribution Practice (GDP) Certificate where appropriate in accordance with ITB Clause 17.6;

Bidder has to submit Description of the organization of the warranty offered in accordance with the conditions laid down in GCC Clause 23

Bidder has to submit Manufacturer Authorization Letter in accordance with ITB Clause 5.6

Bidder has to submit Certificates of satisfactory execution of contracts provided by contracting parties to the contracts successfully completed in the period and budget of at least that of this contract in the past years;