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Format of Forwarding Letter

Format of Forwarding Letter

Format of Forwarding Letter

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GOVERNMENT OF INDIAOFFICE OF THE MEDICAL SUPERINTENDENTSAFDARJANG HOSPITAL, NEW DELHI-110029Rate enquiry for Safdarjang Hospital, New Delhi / Dr. R.M.L. Hospital, New DelhiPrice <strong>of</strong> Form Rs.500/- (Per Group)ADVERTISED TENDER ENQUIRYTENDER NO & DATE : Q-1-MS( 9 ) dt. 29/05/2012BRIEF DESCRIPTION OF ITEMS (Group) : H (Contrast Media )TIME & DATE OF OPENING OF TENDER : 29/05/2012 … 10.30 amAMOUNT OF BID SECURITY : Rs. 1,00,000.00 (Rupees One lakh only)T E R M S A N D C O N D I T I O N SOnly those firms will qualify to compete, who meet the following eligibility criteria1. ELIGIBILITY CRITERIAi. EMD: Earnest money deposit <strong>of</strong> Rs. 1,00,000.00 (Rupees One lakh only) for each group exceptGroup I, and Rs. 25,00.00 for group I, in the shape <strong>of</strong> Demand Draft only, drawn in favour <strong>of</strong> theMedical Superintendent, Safdarjang Hospital, New Delhi should be attached with the tender form,failing which the tender will be rejected. The Tender Number, due date and complete address <strong>of</strong>the firm should also be written on the back <strong>of</strong> the demand draft.ii. DRUG LICENSE: A valid drug license / import License from the drug controller for themanufacture /Import <strong>of</strong> the medicine/drug quoted. A valid drug license / import License from thedrug controller for the manufacture /Import <strong>of</strong> the medicine/drug quoted. If revalidation <strong>of</strong> druglicense has been applied for the copy <strong>of</strong> application to State Drug / Licensing authority may beattached with a certificate that application for renewal was made within time frame as per Drugand Cosmetic Act as amended up to date and that has not been deleted by licensing authorityiii. QUALITY: Manufacturing firms should be registered with the Directorate General <strong>of</strong> QualityAssurance (D.G.Q.A.), or should have Good Manufacturing Practice (G.M.P.) certificate as perRevised Schedule ‘M’ <strong>of</strong> Drugs & Cosmetic Act for indigenous drugs. For imported drugs, goodmanufacturing practice (G.M.P) certificate verified by the State Drug Controller / Drug Controller<strong>of</strong> India. In accordance with the W.H.O. recommendations (in short called WHO – GMPCertificate) should be furnished for the drug/medicine quoted.The firm should clearly highlight the quoted item(s) in the list <strong>of</strong> DGQA / WHO-GMP certificates& Drug license.iv. EXPERIENCE: The bidder should have not less than 2 years <strong>of</strong> manufacturing and marketingexperience for the specified product duly supported by documentary evidence except in case <strong>of</strong>new drugs.v. ANNUAL TURNOVER: The Manufacturing firms should have minimum annual turnover <strong>of</strong> :a. Rs. 50 crores (Fifty crore) for GROUP A -1( higher antibiotics)b. Rs 12 crore (Twelve crores) for GROUP A-2, B, C, D, E, F, G and H (blood products andother items except Misc. Drugs),c. Rs 5 crores (Five crores) for Group-I(The annual audited Balance Sheet <strong>of</strong> the manufacturing firm for the last financial year should beenclosed in all cases).2. SUBMISSION OF BIDSi. The bidders shall submit their bids in two parts in separate sealed covers marked as a)“TECHNO-COMMERCIAL BID” b) “PRICE BID” as the case may be. Both the sealedenvelopes should also have the Tender No., Date <strong>of</strong> Opening, Group <strong>of</strong> Items, name & address<strong>of</strong> the bidder, marked on the sealed envelopes. Both the sealed envelopes should be put in anouter Main Cover which should also be sealed and marked with Tender No., Date <strong>of</strong> Opening,Group <strong>of</strong> Items, name & address <strong>of</strong> the bidder.

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