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.
ii. TECHNO – COMMERCIAL BID : All the documents as mentioned in the EligibilityCriteria, Clause 22 <strong>of</strong> the terms & conditions and check list (enclosed), any other documentwhich doesn’t give an indication <strong>of</strong> the price, List <strong>of</strong> items quoted with specifications /composition <strong>of</strong> the item, pack size etc. should be enclosed in the Techno-Commercial Bid.(THE COLUMN FOR PRICE SHOULD BE LEFT BLANK IN TECHNO – COMMERCIALBID). If price is mentioned in the techno-commercial bid, the bid is likely to be rejected. Thebid should be duly type written, free from erasing/over-writing/cuttings along with a s<strong>of</strong>t copy<strong>of</strong> the same in non convertible PDF format.iii. PRICE BID: List <strong>of</strong> items quoted with specifications / composition <strong>of</strong> the item, pack size etcexactly as submitted in the Techno-commercial bid along with the price <strong>of</strong> the items should beenclosed in the Price Bid (in duplicate). It should be duly type written, free from erasing/overwriting/cuttingsalong with a s<strong>of</strong>t copy <strong>of</strong> the same in non convertible PDF format. The rateswill be valid for a period <strong>of</strong> not less than one year or till new tenders are finalized for nextfinancial year which ever is lateriv. It may be noted that when the main cover is opened on the date and time scheduled for bidopening, only the technical bids will be opened and read out in public.v. Bidders whose techno-commercial bids are found substantially responsive will be informed <strong>of</strong>the date and time <strong>of</strong> opening <strong>of</strong> their price bids. Price bids <strong>of</strong> others will be returned to themunopened before, opening the price bids <strong>of</strong> others. If some <strong>of</strong> the items <strong>of</strong> a bidder aretechnically approved, the price <strong>of</strong> other items which are not approved shall be ignoredvi. The documents should be dropped in the tender box kept at the Ground Floor in Addl D.G.and Medical Superintendents Office, before the date and time <strong>of</strong> the Tender Opening.vii. All the pages <strong>of</strong> tender documents should be properly numbered and total number <strong>of</strong>pages be indicated on the forwarding letter as per format attached.viii. For newly introduced drugs, the manufacturer will be required to submit a certificate <strong>of</strong>marketing from the Central / State Drug Controller / Licensing Authority3. UNDERTAKINGi. The firms should give an undertaking that they are bound to supply the quotedmedicines/drugs within the stipulated time, failure <strong>of</strong> which would render the firm liable foraction as mentioned in clause 15 (i) <strong>of</strong> the tender.ii. The firm is required to submit a certificate in the format as “I / we have read and understoodall the terms and conditions governing the tender. I / we agree to abide by all the terms andconditions <strong>of</strong> the tender enquiry”4. BID OPENINGi. The Tender Opening Committee (TOC) will open bids in the presence <strong>of</strong> bidder’srepresentative, who choose to intend, at the time and date specified in the invitation for bidsand in the following location.OFFICE OF THE MEDICAL SUPERINTENDENTSAFDARJANG HOSPITALNEW DELHI-110029ii.iii.The bidders representatives who choose to attend the bid opening, shall bring with them aletter <strong>of</strong> authority from the bidder on the letter head for having been authorized to be presentat the time <strong>of</strong> opening <strong>of</strong> the bid. In the absence <strong>of</strong> such a a letter <strong>of</strong> authority, therepresentative will not be allowed to present and/or to attend the bid opening. The bidder’srepresentatives who are present shall sign a register evidencing their attendance. In the event<strong>of</strong> the specified date <strong>of</strong> bid <strong>of</strong> opening being declared a holiday for the purchaser the bids shallbe opened at the appointed time and location on the next working day.The TOC will examine the bids to determine whether they are complete, whether required bidsecurity has been furnished, whether the documents have been properly signed, and whetherthe bids are generally in order.