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Note to Vendors:

Reference to the Singapore Healthcare Services Act (HCSA), the Ministry of Health requires all staff of healthcare, regardless public or private healthcare, including personnel from outsourced partners or vendors who regularly work in the healthcare institution premise, to meet the measles and diphtheria immunity requirements by 3rd January 2022.


RFP Type
New
CategoryRFP
Reference No.SCM CGH2023/RFP/K122125
TitleSUPPLY AND DELIVERY OF PRE-FILLED FORMALIN WITH TERM CONTRACT FOR 2 YEARS AND OPTION TO EXTEND FOR 2 YEARS
DescriptionThe Formalin is a kind of fixative which is used to prevent autolysis of the patient's tissue specimen by inactivating lysosomal enzymes and inhibit the growth of bacteria. They also stabilise the cells and tissues to protect them from the rigors of subsequent histology processing and staining techniques. 
Publish Date (DD/MM/YYYY)09/06/2023 10:00 AM
Closing Date (DD/MM/YYYY)23/06/2023 03:00 PM
Extension Date (DD/MM/YYYY)
Tender Box NoWe will be accepting submission of RFP Documents and Annexes via email.
Submission LocationVia email to [email protected] 
Primary ContactPeggy Loh
Tel: 6850 4697
Email: [email protected] 
Secondary ContactN.A
EligibilityN.A
Fees (SGD)N.A
GSTN.A
Document Collection
RFP/RFI/Tender documents are obtainable from the Buyer-in-charge via email: [email protected] 

Interested bidders are to write in to the buyer-in-charge and provide the following information: 
  1. Company full name
  2. Person(s)-in-charge of response to this RFP
  3. Email address & contact number of person(s)-in-charge
Site Showround / BriefingNo
Non-Disclosure Agreement (NDA)Vendors are required to sign a Non-Disclosure Undertaking (NDU) before collection of RFP document. The NDU is to be duly signed by the authorised signatory from the Vendor’s organisation. 
Remarks
Registration of Medical Devices from Health Science Authority (HSA) 

Vendor shall ensure that the medical devices, with the exception of class A exempted should be: 
  1.  registered on HSA Singapore Medical Device Register (SMDR); 
  2. placed on SMDR Transition List ; OR  
  3. cleared for import and supply through one of HSA Product Registration       special access routes 

From 1 Jan 2012, all medical devices, class A, B, C, D, have to be registered with HSA .

We shall reserve our rights not to accept your submission if any Bidder did not adhere to the following instructions:
  1. Submit your RFP proposal ONLY at 60 mins before the RFP closing date & time (for this RFP, Bidder is to submit their proposal only on 23 June 2023, after 1400hrs, BUT not later than 1500hrs).
  2. In the email, Bidder shall perform a print screen the Pricing summary in Part 5 of your RFP document, in order for us to correspond your submission to ensure transparency in recording of price as of closing date and time.
  3. All submissions must be submitted before the closing time and date.
Terms

The terms of this RFP/RFI/Tender have been posted at this site on the published date in their full intent and effect. CGH bears no responsibility for and shall not be bound by any changes made to such terms by unauthorised third parties. CGH does not guarantee that the terms received by you on this site comply with those as originally published. (If you wish to respond to this RFP/RFI/Tender, you are advised to verify such terms directly with CGH.) The Hospital does not bind itself to accept the lowest, the whole or any proposal.