Tender Details
Provision and Installation of Two Autoclaves
Business Name
QIMR Berghofer Medical Research Institute
VP Reference #
VP517477
Buyers Reference #
2026 149
Opens
Friday 17 July 2026 (E. Australia Standard Time)
Closes
Monday 31 August 2026 05:00 PM (E. Australia Standard Time) CLOSED
Supplier query cut-off
Monday 24 August 2026 05:00 PM (E. Australia Standard Time)
Expected decision
Monday 21 September 2026 (E. Australia Standard Time)
Buyer Details
Business Name
QIMR Berghofer Medical Research Institute
Location
300 Herston Rd
Herston, Queensland 4006
Australia
WebSite:
http://www.qimrberghofer.edu.au
Business Info
At QIMR Berghofer, we seek to discover, diagnose and deliver better treatments for some of the world’s deadliest diseases.
Contact Details
The buyer has elected to have their personal and contact details hidden. These details will be revealed at the buyers discretion.
What the buyer is requesting
Details
Supply, Delivery and Installation of Two (2) Laboratory Autoclaves

1. Introduction

QIMR Berghofer Medical Research Institute invites suitably qualified and experienced suppliers to submit an Offer for the supply, delivery, installation, commissioning, and training associated with two (2) Laboratory Autoclaves.

The autoclaves will be utilised as part of QIMR Berghofer's ongoing laboratory operations and will primarily be used for the sterilisation and treatment of laboratory equipment, consumables, and biological waste.

2. Project Overview

The purpose of this Invitation to Offer (ITO) is to source two (2) Laboratory Autoclaves that meet the operational, safety, and compliance requirements of QIMR Berghofer's PC3 laboratory environment.

The successful supplier will be responsible for providing a complete turnkey solution, including all costs associated with:

Supply of two (2) laboratory autoclaves.

Freight and transportation to site.

Delivery and handling.

Installation and commissioning.

Validation and testing.

Integration with existing services where required.

Operator and maintenance training.

Provision of user manuals and technical documentation.

Warranty and ongoing support services.


3. Site Location

The equipment is to be delivered and installed in:

QIMR Berghofer Medical Research Institute

Level 14, Central Building

300 Herston Road

Herston QLD 4006

The installation location is within a Physical Containment Level 3 (PC3) laboratory environment. Suppliers should ensure that proposed equipment is suitable for installation and operation within a PC3 facility and identify any site requirements necessary for installation.

4. Scope of Requirements

The proposed autoclaves should:

Be designed for laboratory and research applications.

Be suitable for sterilisation of laboratory equipment, glassware, instruments, consumables, and biological waste.

Meet all relevant Australian Standards and applicable regulatory requirements.

Include programmable sterilisation cycles and data recording capabilities.

Incorporate user-friendly control interfaces.

Provide appropriate safety interlocks and operator protection features.

Be constructed from materials suitable for laboratory environments with high durability and corrosion resistance.

Include maintenance and servicing requirements as part of the proposal.

Please be aware all organisations planning submissions must attend the Site Visit and briefing.
Background information / Compatibility requirements
Details
Background Information

QIMR Berghofer Medical Research Institute is one of Australia's leading medical research organisations, conducting translational research across areas including cancer, infectious diseases, mental health, population health, and chronic disorders.

As part of its research activities, QIMR Berghofer operates Physical Containment Level 3 (PC3) laboratory facilities that require reliable sterilisation and decontamination equipment to support daily operations and maintain compliance with applicable biosafety requirements.

The Institute currently requires two (2) new laboratory autoclaves to support the sterilisation of laboratory equipment, instruments, consumables, media, and the treatment of biological waste generated through research activities. The autoclaves will be installed within the PC3 laboratory environment located on Level 14 of the Central Building at QIMR Berghofer's Herston campus.

The Institute is seeking a modern, reliable, and energy-efficient solution that will provide safe and effective sterilisation capabilities, minimise operational downtime, and support future laboratory requirements. The proposed equipment should be suitable for intensive laboratory use and capable of operating within a highly regulated research environment.

Suppliers should note that the installation location is an operational research facility with controlled access requirements. It is expected that respondents consider all aspects of delivery, logistics, site access, installation methodology, commissioning, validation, and ongoing maintenance support when preparing their submissions.

QIMR Berghofer seeks a turnkey solution that includes supply, delivery, installation, commissioning, user training, warranty support, and ongoing service capabilities to ensure the equipment remains fully operational throughout its lifecycle.
Desired Outcomes ('Nice to haves', Conditions & Warranties, SLA's, Project benefits)
Details
1. Biosafety and Containment Compliance

Provide effective sterilisation and decontamination of laboratory equipment, reusable materials, and biological waste generated within the PC3 facility.

Support QIMR Berghofer's obligations under the Australian/New Zealand Standard AS/NZS 2243.3 (Safety in Laboratories – Microbiological Safety and Containment) and relevant OGTR and Queensland Health requirements.

Ensure containment integrity is maintained throughout the sterilisation process and during routine operation.

2. Fit-for-Purpose PC3 Solution

Supply autoclaves specifically designed and validated for operation in a high-containment research environment.

Where applicable, provide pass-through/barrier configurations that support dirty-to-clean workflow management and minimise contamination risks.

Meet all applicable Australian standards, workplace health and safety requirements, and manufacturer certifications.

3. Reliable and Efficient Operations

Deliver a robust and dependable sterilisation solution capable of supporting continuous research activities.

Minimise equipment downtime through high reliability, preventative maintenance programs, and responsive service support.

Provide programmable cycles suitable for laboratory waste, liquids, equipment, instruments, and research materials.

4. Verification and Validation

Successfully commission and validate the autoclaves for use within a PC3 laboratory environment.

Provide Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documentation and support where applicable.

Demonstrate and document sterilisation performance to ensure compliance with operational and regulatory requirements.

5. Whole-of-Life Value

Provide a solution that delivers value for money across the equipment lifecycle, including acquisition, operation, maintenance, and support costs.

Maximise equipment longevity, energy efficiency, and ease of maintenance.

Ensure the availability of local technical support, spare parts, and service expertise.

6. Safe Installation and Integration

Complete delivery, installation, commissioning, and validation with minimal disruption to ongoing research activities.

Integrate successfully with existing laboratory infrastructure and utility services.

Ensure all work is undertaken in accordance with QIMR Berghofer's site access, safety, and PC3 laboratory requirements.

7. Training and Knowledge Transfer

Provide comprehensive operator and maintenance training for nominated personnel.

Supply all operating manuals, maintenance documentation, validation records, and technical drawings required for ongoing operation and compliance.
Supplier lists selected
Lists
  • Lab, Measure, Observe & Test Equip
  • Medical Equipment. & Supplies
Categories selected
Categories
  • Laboratory & Measuring & Observing & Testing Equip
    1: Laboratory & Scientific Equipment
  • Medical Equipment & Accessories & Supplies
    1: Medical Equipment & Accessories & Supplies
Regions of Service
Locations
  • Queensland
    1: Brisbane

All Regions of Service locations are within Australia.
Information requested by others
21/Jul/2026 02:27 PM
Question:
Hi Dhwani,

I would like to confirm that Kirthun Ramasingh from Getinge Australia will be attending the site briefing on the 28th July.

Kind Regards

Uma Singh

Getinge Australia Pty Ltd

Answered on 21/Jul/2026 04:01 PM:


Thank you for your confirmation
21/Jul/2026 02:56 PM
Question:
While reviewing the tender documentation, it was noted that the mandatory supplier briefing session is scheduled to be held at 300 Herston Road, Herston QLD 4006 on Tuesday, 28 July 2026. As attendance at this briefing is a mandatory requirement for submitting a tender, I would like to enquire whether an online attendance option is available. If so, when and will there be a link sent?

Answered on 21/Jul/2026 04:07 PM:


Hi Chris

The onsite visit is a mandatory requirement, we believe this is necessary to enable suppliers to gain a full understanding of the site and any potential challenges that maybe presented.

Kind regards

Paul Bensley
24/Jul/2026 10:28 AM
Question:
Hi Team, this is to advise we would be attending the briefing session. Thank you

Answered on 27/Jul/2026 01:59 PM:


Thank you
24/Jul/2026 03:51 PM
Question:
InVitro Technologies will attend site briefing on the 28th July.

Answered on 27/Jul/2026 02:00 PM:


thank you
27/Jul/2026 10:04 AM
Question:
Dear Team,

We only became aware of this tender over the weekend and saw today that a mandatory on-site briefing is scheduled for 28 July.

Unfortunately, our managers and engineers are fully committed this week and are unable to attend the briefing in person. We would like to ask whether it would be possible to receive the briefing materials via email, or alternatively, arrange a separate briefing or site visit sometime next week.

We would greatly appreciate your consideration and look forward to your response.

Kind regards,

Answered on 27/Jul/2026 03:12 PM:


Thank you for your enquiry, I'm confirming we will run another walk through and will provide an update on times and dates tomorrow.
27/Jul/2026 12:30 PM
Question:
Hello, can you please supply proper layout drawing of the site - room’s layout in dwg or pdf with all the available dimensions.

Answered on 28/Jul/2026 12:21 PM:


We will provide drawings for Level 14 by the end of Wednesday 29th August.
27/Jul/2026 12:32 PM
Question:
Hello,

I have another request from the vendor for an extension.

With this level of project complexity and without any DWG drawings, it is practically impossible to properly support you within such a short time.

We are talking about sterilization equipment where we absolutely need to understand the exact installation layout and room configuration, supported by proper DWG drawings and technical details of the site.



Without this information, we are unfortunately not able to properly verify the proposed configuration, utilities, loading/unloading logistics, service accessibility, door orientation, or potential installation constraints.

Is it possible to get extension on the tender.

Answered on 28/Jul/2026 12:20 PM:


Hi Frances thank you for your message. I can confirm we will supply drawings within the next 24 hours. While I can't guarantee an extension will be granted I recommend making a request for the required date, it will be reviewed by the Project Team and accepted or rejected. I hope this helps.
27/Jul/2026 03:23 PM
Question:
Hi all,

after briefing the initial tender document, I scheduled a 10am site visit Tuesday 28th July as noted mandatory and sign in at reception to register attendance.

Further detailed viewing of the document today in scheduled office time has made me aware there was an RSVP for this.

Is it still possible to attend this scheduled site visit tomorrow?

Answered on 27/Jul/2026 03:29 PM:


Thank you for your enquiry, yes we will accept your enquiry as the RSVP even though post the required date.
28/Jul/2026 08:10 AM
Question:
Good morning,

Due to illness, I am unable to attend today's session. I noticed in a previous response that a second session will be held in the near future. Is that upcoming session open to everyone?

Answered on 28/Jul/2026 08:58 AM:


Hi Darren - that's no problem you will be able to attend another event, I'll provide an update today through vendor panel.
28/Jul/2026 03:28 PM
Question:
Hi,

I would like to request an Extension on this project to close at the end of August. This is due to our factory staff currently on summer break in Europe. Thank you for your consideration.

Answered on 30/Jul/2026 08:48 AM:


Hi Uma, I can confirm we have agreed to extend the submission date to 5pm Monday 31st August.
30/Jul/2026 07:56 AM
Question:
Morning, I would like to RSVP to the 11am session on Tuesday 4th August. Thank you.

Answered on 31/Jul/2026 05:46 PM:


Thank you
31/Jul/2026 07:36 AM
Question:
Confirming that we will be attending the walk through on 4th August.

Answered on 31/Jul/2026 05:46 PM:


Thank you
31/Jul/2026 11:25 AM
Question:
Hi,

I would like to confirm Andy Robertson (Projects & Installation Manager) and Jarrod McKay (QLD Service Tech) will be attending the site visit on Tuesday 4th August on behalf of Tecniplast Australia.

Kind regards,

Ian Henton-Smith

Regional Sales Manager

Tecniplast

Answered on 31/Jul/2026 05:46 PM:


Thank you
31/Jul/2026 09:53 PM
Question:
HI Dhwani

Yvette Barden( Biomed Engineer) from our Team will join the tuesday Meeting at 11am


Thanks

Raj

Sales Director Wishmed

Answered on 03/Aug/2026 03:01 PM:


Thank you
03/Aug/2026 01:04 PM
Question:
Good afternoon,

I would like to confirm Jason, Craig and Simon will be attending on behalf of Next Degree tomorrow.

Answered on 03/Aug/2026 02:58 PM:


Thank you
06/Aug/2026 04:34 PM
Question:
Dear Dhwani,

Could you please provide us with the DWG drawings so we can use them to prepare the layout for the equipment?

Kind regards

Answered on 07/Aug/2026 11:25 AM:


Hi Charbel

Thank you for your enquiry, I have uploaded a new file - CENTRAL LEVEL 14 - PC3 FACILITY.DWG - please let me know if there are any issues accessing the information.

Kind regards

Paul Bensley
10/Aug/2026 09:18 AM
Question:
Morning,

Can we please get a floorplan in AutoCAD / DWG Drawing for this tender ?

Thanks

Answered on 10/Aug/2026 02:24 PM:


Hi Felicity

Thank you for your question. My understanding is that the DWG files supplied should be able to be opened in Autocad - please check the last file uploaded. Please message on this platform if there are any specific details you are unable to get from the drawings and I'll get those details and reply.

Kind regards

Paul Bensley
21/Aug/2026 02:19 PM
Question:
• Does the Woods specification document need to be completed or just the Invitation to offer word document?

• Point 3.3.1 With Proposal 2 “Control System Architecture Diagram”. Please confirm if this is the software architecture layout or a P&ID layout?

• Point 4.1.2 Woods Scope document specifies a rubber type barrier seal flange with no joints or splices are permitted as sealed barrier. The invitation to Offer document does not have this specification and it is above the Australian standard AS/NZS 2243.3. Please clarify if this is a hard requirement or not?

• Point 5.2.15 The autoclave shall have the capability to cool hot decontaminated liquid waste from autoclave chambers using supplied cooling water and onboard heat exchanger to a temperature less than 60°C prior to discharge from autoclave boundary. Use of water supplied to the autoclave to cool hot decontaminated liquid waste from autoclave chambers e.g., by direct sparging into hot decontaminated liquid waste from autoclave chambers is not permitted. Is 80 degrees acceptable?

• 5.1.15 Following the end of the autoclave warranty period the Vendor shall be responsible for pressure vessel inspection of the autoclave chamber and rectification of any issues identified during the inspection. Please clarify if this is a hard requirement.

• 5.1.16 Autoclave shall meet AS/NZS 2243.3 requirement of providing an alternative mechanism for decontamination of the autoclave and autoclave load in the event of autoclave fault/failure. Please clarify if the inclusion of H2O2 cycle compatibility via an external generator supplied by QIMR is a requirement?

• 5.2.2 The plant steam of the required quality shall be used in the autoclave chamber for decontamination and sterilisation. The supplier to verify with QIMRB the quality of the plant steam generated. What is the quality of the plant steam?

• 5.7.3 Process cooling water at 6 degrees C. Please confirm if this is a chilled water loop and if QIMR expects to see a chilled water heat exchanger loop system as part of the autoclave offer?

Answered on 27/Aug/2026 03:58 PM:


Hi Ian

Please see the response below - we are still waiting on additional information which I'll update as soon as I have it. Thank you for your patience.


Does the Woods specification document need to be completed or just the Invitation to offer word document? Please ensure your response is made within the Invitation to Offer Document rather than the Woods specification document.

• Point 3.3.1 With Proposal 2 “Control System Architecture Diagram”. Please confirm if this is the software architecture layout or a P&ID layout? All approved layout options are listed in 3.3 (section above 3.3.1) “The Vendor shall provide the documents listed in the following document schedule.

Design documentation shall be issued to the Client in the following file formats:

• Project Schedules in PDF format.

• Lists / Schedules in PDF format and in MS Excel.

• P&ID’s in PDF and .dwg format.

• 3D Models in .stp or .dwg format.

• Functional Specifications in PDF format and in MS Word

All PDF files shall be indexed and character searchable.

The size of drawing sheets shall be in accordance with the ISO-A series and all drawing sheets shall include grid references.”


• Point 4.1.2 Woods Scope document specifies a rubber type barrier seal flange with no joints or splices are permitted as sealed barrier. The invitation to Offer document does not have this specification and it is above the Australian standard AS/NZS 2243.3. Please clarify if this is a hard requirement or not? Please follow the Wood specification as this is what will meet the PC3 certification requirements. If this is not possible, please explain why and what measures you would take to ensure the standard is met for the PC3 laboratory certification requirements (TGA, OGTR and DAFF).

• Point 5.2.15 The autoclave shall have the capability to cool hot decontaminated liquid waste from autoclave chambers using supplied cooling water and onboard heat exchanger to a temperature less than 60°C prior to discharge from autoclave boundary. Use of water supplied to the autoclave to cool hot decontaminated liquid waste from autoclave chambers e.g., by direct sparging into hot decontaminated liquid waste from autoclave chambers is not permitted. Is 80 degrees acceptable? Please follow the required temperature listed. If this is unattainable, what safety measures are included to ensure operator and staff safety.


• 5.1.15 Following the end of the autoclave warranty period the Vendor shall be responsible for pressure vessel inspection of the autoclave chamber and rectification of any issues identified during the inspection. Please clarify if this is a hard requirement. Yes, before the end of warranty a final service/inspection should be undertaken and any issues rectified at no charge.

• 5.1.16 Autoclave shall meet AS/NZS 2243.3 requirement of providing an alternative mechanism for decontamination of the autoclave and autoclave load in the event of autoclave fault/failure. Please clarify if the inclusion of H2O2 cycle compatibility via an external generator supplied by QIMR is a requirement? To be checked and confirmed by the design team

• 5.2.2 The plant steam of the required quality shall be used in the autoclave chamber for decontamination and sterilisation. The supplier to verify with QIMRB the quality of the plant steam generated. What is the quality of the plant steam? To be checked and confirmed by the design team

• 5.7.3 Process cooling water at 6 degrees C. Please confirm if this is a chilled water loop and if QIMR expects to see a chilled water heat exchanger loop system as part of the autoclave offer? To be checked and confirmed by the design team
Updates made to this Request
20/Jul/2026 08:09 AM
Please note: The following attachment has been recently added.

1. Added: invitation-to-offer-2026 149 Autoclaves (HM160726) (003).docx

Please consider this attachment when responding.

28/Jul/2026 03:32 PM
Please note: The following attachment has been recently added.

1. Added: CENTRAL LEVEL 14 - PC3 FACILITY.pdf

Please consider this attachment when responding.

28/Jul/2026 03:39 PM
Dear Suppliers,

Please be aware we will be running another walk through at 11am on Tuesday 4th August. This is being made available for those interested in making a submission but who could not attend the first walk through and those who did make the walk through but would like to attend again. Please RSVP through vendor panel before 2pm Monday 3rd August.

28/Jul/2026 04:20 PM
Dear Suppliers,

Given we are running a second walk through next week and that Northern Hemisphere suppliers are impacted by their vacation season we are extending the submission date to 5pm Monday 31st August 2026.

07/Aug/2026 11:22 AM
Please note: The following attachment has been recently added.

1. Added: CENTRAL LEVEL 14 - PC3 FACILITY.DWG

Please consider this attachment when responding.

31/Aug/2026 09:47 AM
Please note: The following attachment has been recently added.

1. Added: Supplimentary Question 1 31.08.2026.docx

Please consider this attachment when responding.