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K120123

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 TypeNew
CategoryRFP
Reference No.SCM CGH2023/RFP/K120123
TitlePROVISION OF AFTER-OFFICE-HOURS CLINICAL HOME SERVICES FOR PATIENTS-AT-HOME PROGRAMME WITH A TERM CONTRACT OF 1 + 1 (OPTION) YEARS.
DescriptionThis RFP is called to provide clinical care to patients in their respective locations of residence, where they have been enrolled into the Client’s CGH@ Home programme.

Full details to be referred to Part 4: Scope and Specifications
Publish Date (DD/MM/YYYY)15/03/2023 10:00 AM
Closing Date (DD/MM/YYYY)29/03/2023 03:00 PM
Extension Date (DD/MM/YYYY)
Tender Box NoVia email to: [email protected]
Submission LocationVia email
Primary ContactMs Dyllis Lee
Tel: 6850 4776
Email: [email protected]
Secondary ContactMs Elina Ee
Tel: 6850 4765
Email: [email protected]
EligibilityN.A.
Fees (SGD)N.A
GSTN.A
Document CollectionNo collection of document from CGH office is possible. Interested bidders shall request for the RFP documents by writing to the buyer-in-charge with the following information:

  1. Name of Bidder Company:
  2. Person/s in charge of Responding to this RFP:
  3. Email Address of Person/s in charge:
  4. Mobile Number of Person/s in charge:

The RFP documents will be emailed out to Bidders who had written in with the above information.
Site Showround / BriefingNo
Non-Disclosure Agreement (NDA)N.A.
Remarks Registration of Medical Devices from Health Science Authority (HSA)
Vendor shall ensure that the medical devices, with the exception of class A and B, delivered on or after 1 Aug 2010 to 31 December 2011 should either 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 SMDR.
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.