TENDER RATE CONTRACT FOR SUPPLY OF IV IG & INJECTABLE ANTIBIOTIC FOR BIMS BELAGAVI

GST Registration Certificate.

PAN Card.

Original Certificate of Incorporation signed by the Registrar of Companies (ROC) in case of a company/firm. Original proprietorship Certificate in case of a proprietary firm.

Annual Turnover Statement Certified by Commercial Tax Officer/ Chartered Accountant. 2022-23, 2023-24, 2024-25 For Mfr: 5 CRORES / ANNUM For Supplier: 2 CRORES / ANNUM

Annual Turnover Statement Certified by Commercial Tax Officer/ Chartered Accountant 2022-23 2023-24 2024-25 For SSI MSME NSIC 2.5 CRORES ANNUM

If the Tenderer is an Authorized Agent/Distributor, the copy of Manufacturers Annual Turnover Statement along with his Annual Turnover certified by Commercial Tax Officer/Charted Accountant 2022-23 2023-24 2024-25

Balance Sheet. 2022-23, 2023-24,2024-25

Profit and loss Account. 2022-23, 2023-24,2024-25

Income Tax Returns (financial year). 2022-23, 2023-24,2024-25

Original/ Notarized Copy of the Manufacturer License along with product permission.

third-party independent testing laboratory which shall not be a part of the manufacturing unit or not owned by the manufacturer/ bidder. Only for IV fluids.

Original/Notarized Copy of manufacturers manufacturing license of his product Quoted If the Tenderer is an Authorized agent /Distributor

Original / Notarized copy of Import License in respect of imported items. The Import License should be valid for at least preceding three years without break.

In case of Imported IVIG & ANTIBIOTICS WHO GMP certificate should be uploaded and the copies shall be attested by the licensing authority/ Notarized.

If Tenderer is an authorized agent / distributor. Original Notarized copy of up-to-date wholesale license issued under Drugs & Cosmetics Act along with products deal

List of items supplied to various Govt./Quasi Govt./Autonomous Institution with quantities during the financial years. 2022-23, 2023-24, 2024-25

If the Tenderer is an Authorized agent / Distributor should upload the copy of Manufacturer Authorization Letter.

Original / Notarized copy of latest Non-Conviction Certificate not older than 6 months in respect of the Manufacturer/ Authorized agent/ Distributors/Importer issued by the Drugs Controller.

If the Tenderer is an Authorized agent/ Distributor should also upload the Original/ Notarized copy of Manufacturers Non-Conviction Certificate.

List of items quoted.

Tender Offer Form.

Tender Declaration Form.

FFS/BIS/ISI/ISO/WHO-GMP/Revised Schedule M-GMP certificates, wherever applicable

Seal & Signature on Tender Documents by the Authorized Signatory.

Each tenderer must upload the Wholesale Market price of each item quoted for supply in a separate format/ annexure.

Self-Declaration Form -For Uploaded Tender Documents (Product Wise)

SSI /MSME/ NSIC Certificate if any

The undertaking in the letter head of manufacturer as well as authorised dealer shall be uploaded stating The NABL accredited laboratory name, address, for the purpose of this tender, means a third-party independent testing laboratory which shall not be a part of the manufacturing unit or not owned by the manufacturer/ bidder. Only for IV fluids.

The undertaking for the below shall be uploaded with details of NABL Lab.NABL accredited lab - the testing laboratories duly recognized by the national accreditation board for testing and calibration laboratories (a constituent board of quality council of india) for the technical competence for performing the specific tests with reference to international standards. such laboratories should have NABL accreditation in relevant disciplines separately to perform quality tests for the tested category of items and shall be duly approved by the D&C Act, in case of drugs. the NABL accredited laboratory should furnish certificate of analysis as per form 39 of d & c rules- Only for IV fluids.

If the bidder is manufacturer should hold valid WHO-GMP certificate who-good manufacturing practices) in respect of the production units and the products quoted. If the offered products are manufactured from more than one unit all the units shall be WHO-GMP certified should be uploaded.or If the bidder is authorised dealer/ distributor than bidder should upload the manufacturers valid WHO-GMP certificate (who-good manufacturing practices) in respect of the production units and the products quoted. If the offered products are manufactured from more than one unit all the units shall be WHO-GMP certified should be uploaded.

The MSMEs registered within the state of Karnataka shall hold valid cGMP certificate issued by the licensing authority for the products manufactured within the state Karnataka.