Permethrin 5% 10gm Cream

OEM or their authorised dealer with valid authorization from OEM provided that OEM should be registered with Medical Department of Indian Railways(For Part I items)/ PCMD,NR,NDLS(For Part II Items) are eligible to participate in tender. Please mention MRP and the name, contact number, email id and address of the supplier and manufacturing unit. Manufacturing unit should have been inspected and declared fit by Indian Railways. Attach relevant documents in reference to all above and copy of outer cover and product of drug. Bids without relevant documents/information are liable to be passed over.

In terms of clause as per Para 2.4.3 of Instruction to Tenderers regarding restrictions on procurement form a bidder of a country which shares a land border with India. I, hereby confirm that I have read the clause regarding restrictions on procurement form a bidder of a country which shares a land border with India and I certify that I am not from such a country.

In keeping with the Public Procurement (Preference to Make in India) Order, 2017,as amended, the procurement is restricted from Class- I & Class-II sources as per Para 2.4.2 of Instructions to Tenderers for Electronic tenders ITT_Rev_1.21_April_2024 along with Correction Slip No.01. Please enter the percentage of local content in the material being offered, enter 0 for fully imported items, and 100 for fully indigenous items. The definition and calculation of local content shall be in accordance with the Make in India policy.

Please enter the percentage of local content in the material being offered. Please enter 0 for fully imported items, and 100 for fully indigenous items. The definition and calculation of local content shall be in accordance with the Make in India policy as incorporated in the tender conditions.

Consignee after receipt.

i) To meet the Eligibility Criteria, various strength of the same salt will be regarded as same product. However, different.types such as capsules, tablet, syrups etc. will be regarded as separate product. (For example- Capsule Amoxicillin 250 mg, 500 mg, 1 gm will be regarded as one product Injection Amoxicillin %F6f various strength will be regarded as one product). ii)Each strip/ packet bottle that contains the tendered item should have a printing/ stamping with indelible ink of 'Northern Railways - Not for Sale' Firms are advised to put their Hologram on their products/ cartons. However, for vitems procured under urgency or on local purchase basis.Purcaser reserves the right to accept the material item/ supplies without the label of 'For Northern, Railways- Not for Sale' by way of issue of necessary amendment to the PO in, this regard.. In such cases, stamping may be done by the consignee before use.

i) The remaining Shelf life of the offered product should not be less than 80% of total Shelf life or it should not. be older than 06 months from the date of manufacture (whichever is more) at the time of supply. In specific cases, CMM/ PCMM may relax this condition on case to case basis with the written undertaking by the tenderer that they will replace unused quantity free of cost before the %E9xpiry of Shelf life of that item with fresh batch. i.a) Non-replacement on free of cost basis of such unused quantities shall tantamount to breach of contract and shall be reported to the Firm Registering Authority.

i) The material shall be inspected by consignee or authorized representative of the consignee on receipt of the material in the hospital. The material may also.be subjected to tests in Railway/ Govt./ Govt recognized-laboratory on random basis or whatever found necessary by the concerned consignee. Page 2 of 4 9.1 Analysis report for laboratory/Govt. Recognized laboratory must accompany the consignment without fail on supply Without of each batch of medicine(s). Product Analysis/ Performance/ Compliance report (wherever & whenever applicable), supplied product will not be accepted by respective consignees. The firm will submit report of the item at the time of supply to the respective consignee, in standard format, that "this product has been, analyzed and found to be conforming to the each batch from manufacturer's own standards". i.a) Whenever on analysis, it is found that items supplied are not conforming to standards, the firms/suppliers are required to replace the whole batch free of cost with another batch to all the consignees, irrespective of whether the batch has been used completely/partially or not. i.b) After the item has been supplied to the Railway, subsequent analysis cost shall be borne by the Railway. However, if the item on lab analysis is found to be sub-standard, cost of lab test shall be borne by the concerned supplier. i . c ) The supplier can. be asked:to replace such sub-standard batch of supply at any time.

a) The item should not be older than six months or item must have a residual shelf life of more than 80% at the timeof supply. b) Whenever drug samples on analysis are found to be not conforming to the standard. The suppliers are required to replace the whole Quantity.

Stamping' northern railway supply not for sale' mentioned on material.