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Suppliers' Guide

About the Catalogue


This guidance details how to sell digital products (Solutions) to the NHS using the Buying Catalogue, including related framework information and Supplier obligations. As of 2019, the Buying Catalogue will include services for primary care, but in the future its scope will expand to cover other care settings. We recommend you read this guide in its entirety before submitting your Solution to the Buying Catalogue.

About the Catalogue

The Buying Catalogue is a procurement platform where clinical commissioners and other NHS buyers can find, evaluate and purchase digital products and services (Solution­s) intended to support GP IT. To be listed on the Buying Catalogue, all Solutions must successfully demonstrate compliance with relevant NHS Standards. In order to sell from the Buying Catalogue, Solutions also must have been awarded to a framework.

Frameworks supported

Although GP IT Futures Framework 1 is the first to be facilitated through the Buying Catalogue, the site is open to any other public sector bodies wishing to introduce new frameworks to the healthcare market.

GP IT Futures Framework 1

GP IT Futures Framework 1 is the first framework to be facilitated through the Catalogue. This framework is open to all Suppliers that provide one or more Capabilities specified in the framework.

The invitation to tender for GP IT Futures Framework 1 will be published in the Official Journal of the European Union (OJEU). It will be published on Bravo (see ‘View our live opportunities’) at the same time.

Benefits of adding your Solution to the Buying Catalogue

Visibility - The Buying Catalogue will be accessed frequently by digital service buyers within the NHS and many other organisations.

Catalogue assured - By achieving compliance with NHS Standards, you can provide confidence to buyers that your Solution is reliable and safe for use in the NHS.

Interoperability - GP IT Futures Framework 1 contains the Interoperability Standard. Achieving compliance with this allows your Solution to work with any other Solutions that also comply with this Standard. Buyers have overwhelmingly expressed a preference for systems that work together.

Is my Solution appropriate for the Buying Catalogue?

GP IT Futures Framework 1 is open to any Solution that can meet at least one of the Capabilities, and the applicable Standards. We strongly recommend that you review the Capabilities & Standards Model to check that your Solution would be appropriate for this framework.

Please note that all Solutions must meet the overarching Standards, regardless of the Capabilities chosen. See Introduction to the Capabilities & Standards Model below.

How long until I can start selling?

In order to sell you need to meet two requirements: (1) have your Solution accepted on the Catalogue as compliant see the ‘Catalogue On-boarding Process’ in Bravo (click ‘View our live opportunities’ and ‘Digital Buying Catalogue Registration’ opportunity); and (2) be awarded to a framework. The order of these two things may vary, but you must have submitted your Solution to the Catalogue and have it accepted into the assessment process in order to qualify for a framework award.

You may start adding a Solution to the Catalogue at any time. See Supplier registration below for how to get access to the Catalogue.

The time it takes for a Solution to be accepted on the Catalogue will vary depending upon the number of Capabilities and Standards involved, and the quality of the initial submission. If all the Standards evidence is submitted by the time the Capability assessment is complete, the aim is that a good quality submission will take no longer than 19 weeks. See a break-down of the Catalogue timescale targets by stage in Process overview below.

(Please note that during preliminary private beta, timescale targets may vary, and the Traceability Matrices for submitting evidence of Standards will be made available as soon as they are ready.)

The framework timescales will be clear at the time each framework is published.

Process overview

All companies need to register one time in Bravo to gain access to the Catalogue. After this, there are four stages to adding each Solution to the Catalogue. The table below provides a brief overview of each stage.

(Please note that during preliminary private beta, timescale targets may vary.).

0. Supplier Registration

What you do What we do

On Bravo

First, register on Bravo if you have not already done so.

Provide your company information.

Sign Catalogue Agreement.

Provide list of staff to be given log-in access under your company account.

On Bravo

Review your submitted Catalogue Agreement.

Notify you when we have accepted your Buying Catalogue Agreement and send you the counter-signed copy of the Agreement.

Upon accepting the Agreement, create user accounts and provide log-in details for staff requiring a Buying Catalogue account.

The aim is that you will have your user logins no longer than 9 Working Days after submission of your Catalogue Agreement, company information and user log-in request.

(Please note that during preliminary private beta, timescale targets may vary.).

1. Provide basic details and select Capabilities*

What you do What we do

On the Catalogue

Provide basic details and key contacts for your Solution.

Select the applicable Capabilities. Your Solution will be assessed against these in the next stage.

Via email

Submit Associated Services and Additional Services. Submit service levels now or at stage 3. Email all submissions to

* If your Catalogue Solution includes the Productivity Capability, you will need to follow an additional process. See Annex 1 of the 'Catalogue On-boarding Process' in Bravo (click ‘View our live opportunities’ and 'Digital Buying Catalogue Registration' opportunity).

When you complete stage 1, you can progress to the next stages as soon as you're ready.

2. Provide evidence of Capabilities*

What you do What we do

On the Catalogue

Evidence how your Solution meets the Capabilities by submitting video or request to present to us via a live witness demonstration.

Via email

Respond to any clarifications if we send them.

Receive outcome of Capability assessment.


On the Catalogue

Review your Solution details.

Review your Capability selection.

Off the Catalogue

Review your Associated Services and Additional Services.

Review your Service Levels, if provided.

Via email

Notify you if your submission has been accepted.


On the Catalogue and/or via live witness demo, as requested

Assess your Capability evidence.

Assess your Associated Services and Additional Services.

On the Catalogue

Update Catalogue with outcome status following our assessment.

Via email

Ask any clarification questions if we have them.

Notify lead contact of Capability assessment outcome.

* If your Catalogue Solution includes the Productivity Capability, you will follow an additional process. See Annex 1 of the 'Catalogue On-boarding Process' in Bravo (click ‘View our live opportunities’).

The aim is that stage 2 will take no longer than 20 Working Days from receiving your evidence or completion of the live witness demo. You can progress to the next stage and submit evidence for Standards while you wait for the outcome of your Capability assessment.

(Please note that during preliminary private beta, timescale targets may vary.).

3. Provide evidence of Standards*

What you do What we do

On the Catalogue

Download, complete and submit Traceability Matrices for your Standards.

Respond to feedback from us. This may include providing more information where required and working with us as we test each Standard against the requirements.

Via email

Submit service levels to if not already provided.

On the Catalogue

Review and provide feedback on evidence for each Standard submitted for compliance.

Via email

Send notification for each Standard when feedback is available.

Send notification for each Standard when compliance is achieved.

Send notification for Solution when compliance with all Standards is achieved.

* If your Catalogue Solution includes the Productivity Capability, you will follow an additional process. See Annex 1 of the 'Catalogue On-boarding Process' in Bravo (click ‘View our live opportunities’).

Once we begin reviewing your Traceability Matrices, the aim is for each Standard to take no longer than 12 weeks including dialogue. This assumes an initial good quality submission. See Annex 1 of the 'Catalogue On-boarding Process' in Bravo (click ‘View our live opportunities’ and 'Digital Buying Catalogue Registration' opportunity) for more detail on this stage.

(Please note that during preliminary private beta, timescale targets may vary.).

4. Build Solution page (what buyers will see)

What you do What we do

On Bravo

For your first accepted Solution, complete and submit the Supplier specific schedules associated with the Catalogue Agreement.

For each Solution, complete and submit the Solution specific aspects of the Catalogue Agreement.

On the Buying Catalogue

Answer questions required to populate this page.

Preview and send page for moderation.

Publish page once moderation, and any necessary changes, are complete.

On the Buying Catalogue

Moderate the detail provided.

Via email

Send outcome of moderation to lead contact.

The aim is you will hear from us within 5 Working Days from submission of your Solution page.

Supplier registration and Catalogue access

Before you can begin adding your Solution to the Catalogue, you must register your company and request a user account as follows:

Log in to Bravo. You will see multiple opportunities listed. Click on the ‘Digital Buying Catalogue Registration’ opportunity.

From there, you can download, review and sign the Catalogue Agreement which sets out the terms of use for using the Catalogue. When you’ve reviewed and gotten the necessary signature, you can upload the signed Agreement to Bravo.

Bravo will also ask you to provide company information (see the 'Supplier checklist' for details), and the names and email addresses of anyone who will need access to the Buying Catalogue under your company account.

Once we have signed the Catalogue Agreement, we will issue log-in details for each of the users requested.

When you receive the log-in details, you can navigate to the Buying Catalogue and click ‘Log in.’ From there, use password recovery and follow the instructions to create your password. You can then log in using this email and password.

Introduction to the Capabilities & Standards model

The scope of services supported by the Buying Catalogue is defined by the Capabilities.

What are Capabilities?

The requirements to deliver Solutions are grouped into Capabilities. Each Capability describes a business need at the highest level. For example, 'Recording Consultations' describes the need for staff to be able to make a digital record of any consultation with a patient. The introduction of Capabilities is intended to allow Suppliers to innovate by being less prescriptive and to segment the requirements in a way to allow more flexibility and choice for buyers.

How is the model structured?

Requirements are grouped into Capabilities. There are different types of Capabilities. There are Capabilities to support business continuity from the previous framework, GPSoC, and new Capabilities to support new ways of working. Six of the business continuity Capabilities have been designated as Foundation Capabilities. Foundation Capabilities have funding implications (see below.)

There are overarching Standards, which are applicable to all Solutions (for example, Information Governance).

There are two types of Standards associated with Capabilities:

• Capability-Specific Standards  are specific to a Capability and usually have the same name (for example, Prescribing);

• Context-Specific Standards sit under and apply to certain Capabilities (for example, Common Reporting).

There is also an Interoperability Standard. Some elements of the Interoperability Standard apply to all Solutions, while other elements are associated with specific Capabilities.

For more detail, see the Capabilities and Standards Model.

Do I have to build a Solution that delivers all Capabilities?

You do not have to provide a Solution that delivers all Capabilities. You may submit a Solution that meets just one Capability, or many. By looking at the Capabilities, you can see where your product portfolio fits. You may want to make tweaks to your existing products so that a Solution will fully match one Capability or a set of Capabilities. Or you may wish to create new Solutions to deliver a broader set of Capabilities.

How do buyers fund their purchases?

Buyers can fund their purchases using central or local funding, or a combination of the two. For buyers to access GP IT central funding, they must first agree a contract for a Solution, or set of Solutions, which provide all of the Foundation Capabilities (model). The Foundation Capabilities form the foundation for a clinical system Solution and are the basis of support for the commitments in the General Medical Services contract. 

Your Solution will be assessed to determine whether it (or a group of your Solutions) forms a Foundation Solution Set. If your Solution is recognised as a Foundation Solution, it will be subject to a maximum list price. If a buyer has purchased all of the Foundation Capabilities, they can use any remaining central funding to buy other Solutions that fulfil other Capabilities. Otherwise, buyers will use local funds to pay for their purchase.

Please review our Capabilities and Standards Confluence site for more information.

Stage 1⏤Solution details

You must provide basic details and select the applicable Capabilities. For specific information required in this stage, see Supplier checklist. 

Please be aware that during private beta, once you complete stage 1, your Solution name and Solution version cannot be changed. If you’ve made an error, please email us.

Before you select applicable Capabilities, we recommend that you review the full Capabilities & Standards Model to understand the relationship between Capabilities and Standards, as well as the requirements under each Capability and Standard.

Stage 2⏤Capability assessment

Submitting Capability evidence

You must submit evidence demonstrating how your Solution meets the Capabilities you have selected. Your evidence will be reviewed to determine if each Capability has been successfully met.

Please note that successful completion of Capability assessment does not mean your Solution has been assured against NHS Standards. Solutions will not receive Compliant Status until successful completion of the Capability assessment and Standards compliance stages, and acceptance of your Solution page.

Once your Solution has achieved Compliant status and been awarded to a framework, you will be able to sell your Solution on the Catalogue.

Within each Capability, there are Epic-level user stories that describe business activities which are facilitated by a digital Solution. For some Capabilities, all Epics are required for the Solution to pass the assessment for that Capability. For others, only one or more Epics are required.

In order to pass an Epic, all of the acceptance criteria under that Epic will need to be demonstrated in the evidence submission. Before you prepare and submit your evidence, you may wish to read Assessing your Capabilities below.

For each Capability, the Supplier can choose whether to provide:

• A recorded video demonstration (with optional voiceover describing what is happening and where each acceptance criteria is met); or

• Schedule a live witness demonstration. During the live witness demonstration, the Supplier will present the Capability. The video will be recorded, and then assessed.

Recorded video demonstrations

The production quality of the video files provided will not be assessed. Your videos can be recorded simply, for example, using a software such as Web-ex, and recording a shared screen. The important thing is that the video provided is clear and easy to view. To this end, including the Epic or Epics included in each video file name will be appreciated.

Narration—either verbal via voiceover or embedded via words on-screen—should be included in each video to indicate where each acceptance criterion is evidenced in each video.

When you submit your videos on the Catalogue, you are required to tell us where in each video each Epic is evidenced. There is a free text field for each Capability where Suppliers can enter, for example, Epic 1 at 2:34.

Please be aware that once you submit your evidence, you cannot change it. If you have submitted evidence in error, please email us.

Can I submit one video that displays all of my Solution's Capabilities?

Your videos can display as many Capabilities as you wish, as long as you clearly demonstrate that your Solution meets the acceptance criteria for each Epic you are including.

My Solution meets a large number of Capabilities, can I submit multiple videos?

You can submit one or multiple video files for each Capability. If you wish to submit multiple videos for a Capability, you can combine these together in a zipped file before uploading. We recommend making the file(s) as small as possible as upload times may be slow during private beta.

What if I don't have any video recording software?

You don’t need specialised recording software. For example, you can create and record a screencast using Web-ex or other meeting application or software.

If you are not able to create videos, you can schedule a live witness demonstration with us.

Will my videos be shown to the public?

Your video evidence will only be used for assessment and will not be published publicly on the Catalogue or elsewhere. However, all information submitted to the Buying Catalogue is subject to FOI requests.

Assessing your Capabilities

Once you have submitted your Solution details and Capability evidence, we will review your submission, including mapping information provided and the applicability of the Associated Services. If we have questions, we will email your lead contact for clarification. Once we have completed our review, we will notify your lead contact of the outcome. If your Solution has been accepted, it will have the status of Catalogue Solution Submission Accepted. If your Solution has not been accepted, you can try again by submitting a new Solution.

At this point, we will assess your Capability Evidence. During this time, we may need to ask clarification questions and request more information to complete our assessment. These clarifications will be sent via email to your lead contact, during private beta.

Each Capability has Epics, and each Epic has acceptance criteria. Each of these acceptance criteria will be reviewed and scored as passed or failed. To pass an Epic, all acceptance criteria for that Epic must be passed.

Epics are labelled as ‘May’ or ‘Must’. For some Capabilities, we will allow and assess partial delivery (one or more but not all Must Epics met) of a Capability, while others have to be delivered in full (all Must Epics met).

Each Capability is clearly marked in Confluence to show if partial delivery is accepted. For these, assessment against a subset of the Epics (and their associated acceptance criteria) is allowed. If the Solution passes with a subset if Epics, these will be marked with a status of Partial Capability.

For those where Partial Capability is not accepted, all Epics and acceptance criteria will be required to pass the Capability. If the Solution passes, these will be marked with a status of Full Capability.

It is possible for a Solution to have a combination of Full Capabilities and Partial Capabilities.

Some Capabilities also have May Epics, which are optional and not required to pass a Capability. Suppliers have the option of including these Epics as part of their evidence submission. If a May Epic is included, it will be assessed in the same way as a Must Epic.

Once we’ve completed our assessment, your lead contact will notified of the outcome.

Stage 3⏤Standards compliance

How to submit evidence - Traceability Matrices

After you’ve submitted evidence for Capabilities (stage 2), you can submit evidence for Standards (stage 3). This stage will involve a detailed analysis of your Solution against each relevant Standard—the overarching Standards, which apply to all Solutions, and the Standards associated with the Capabilities selected.

Each Standard has a separate Traceability Matrix (TM), which is an Excel file that lists each piece of required evidence for that Standard as an individual line item. Based on the risk-based approach outlined below, each line item has been classified as either ‘Must’ (mandatory to implement) or ‘May’ (optional to implement), as defined in the Capabilities and Standards glossary.

You can submit most evidence for a Standard via its TM. Additional files such as screen shots or supporting documents can be included with your TM submission. The TMs for each Standard applicable to your Solution can be accessed via your Standards Dashboard. Each standard will open on its own page. Click on each Standard to download the TM for that Standard. Once you’ve finishing filling in the required information, you can upload the completed TM on the same page. You can submit TMs for each Standard one at time. If you have multiple files to submit, you can zip them into a single compressed file, and upload the zipped files to the Catalogue.

Each Standard can be assigned a ‘Standard owner.’ By default, Standard owner will be your lead contact. You can change the owner to any other authenticated user at your company. (Authenticated users are those for whom you requested access in Bravo when registering your company). Standard owners are typically the ones submitting evidence for that Standard, and will receive all email notifications, along with the lead contact.

Compliance memory

Some Solutions will not start with blank Traceability Matrices on the Catalogue. All eligible Catalogue Solutions will have their existing compliance memory transferred by the Catalogue Authority into the Traceability Matrices to which their Solution maps. Any gaps between previous requirements and the current requirements will be highlighted as a compliance gap for the Supplier to address in its submission.

Eligible Solutions may include, for example, Solutions previously on the GPSoC framework or Solutions compliant with NHS Spine requirements.

It is intended that any evidence submitted on the Catalogue for compliance will be used for future compliance, and that previous compliance evidence will be inherited wherever possible.

Evaluating your Standards

The evidence you submit within your Traceability Matrices (TMs) will be evaluated for compliance, according to the risk-based approach outlined below.

Once we’ve evaluated each line item in a Standard, we will send a notification to the lead contact and Standard owner, linking to our feedback within the TM on the Catalogue. The feedback is intended to support the Supplier in providing additional evidence. Suppliers can re-submit TMs as many times as needed until all line items meet the minimum level required to pass compliance for that Standard.

Compliance approach - risk based

In order to establish our compliance criteria for each Standard, a risk-based approach has been applied to all aspects of each Standard, to determine what level of compliance evidence will be assessed by us, and which areas will be assessed by the buyer.

In general, central compliance will be applied when risks exist around the following areas:

• Clinical safety

• Information governance (including information security)

• Central Spine Services and associated services

• Interoperability

Where central risk mitigations have been identified, a risk level impact has been applied and mapped to mitigating actions. Examples of Standards’ risks/mitigations are shown below:

• No risk impact: yes/no self-certified response

• Low risk impact: a self-certified* statement with a brief description of how you have met the line item

• Medium risk impact: self-certified* statement with an implementation description plus physical evidence which may include screenshot/video, API response message, evidence of external compliance/certification (for example, ISO)

• High risk impact: witnessed tests, design documents

The compliance evaluation of your overarching Standards will also seek a proportionate risk-based approach. However, given the nature and variability within the overarching standards, the approach will be dependent on an understanding of the Solution being provided.

Compliance approach – ongoing

Ensuring that Solutions remain compliant to Standards post-evaluation is critical to provide buyers with assurance that Solutions continue to function as intended and do not present safety risks. All Catalogue-assured Solutions must follow the requirements in the Service Management Standard, which will explain how Suppliers should manage change to their Solution, including any related compliance activities, for example, change and regression testing.

Suppliers will have a responsibility to cooperate with any feedback activities or direct audits. The goal of both activities is to help identify and address any non-compliance and support the continued delivery of compliant Solutions to end users.

Stage 4⏤Solution page

This stage is not yet available to start. All lead contacts that have Solutions in progress on the Catalogue will be notified as soon as it is available.

Having successfully passed both the Capabilities assessment and the Standards compliance stages, you can progress to populating your Catalogue Solution listing, which will form your Solution page. In this final stage, you will be asked to provide additional information relevant to potential buyers. For specific information, see the Supplier checklist.

Some aspects of the Solution page may vary by framework, for example prices and performance levels.

We will moderate the Solution page to ensure it appears factually correct, isn’t misleading, and is presented within the spirit of the Commercial Standard before you can publish it.

Contact us

Catalogue submissions

To submit Additional Services, Associated Services and service levels for your Catalogue Solutions, or to ask questions about your submissions, email the Catalogue support team at

All other questions

For any other Catalogue questions, errors or issues experienced when using this website, email the NHS Digital service desk at, or call at 0300 303 4034.

Supplier checklist

To help Suppliers to prepare for Catalogue submissions, this section lists each piece of information required or requested by the Catalogue at each stage. All information is added by the Supplier, with the exception of certain Solution page information. In the Solution page section, we will pull across or copy over information entered previously on the Catalogue or on other platforms, such as framework information and pricing. See detail below.

All fields mandatory unless otherwise indicated.

Stage Field name Description Visibility

Supplier registration

Signed Catalogue Agreement

This is in Bravo. Someone from your company will need sign the Catalogue Agreement, and it will need to be accepted by the Catalogue Authority, before anyone from your company can access the Catalogue.

Catalogue Authority

Supplier registration

Company name

This is in Bravo. We will use company name to identify your organisation along with its DUNS number. We will also register individuals for whom you’ve requested access under the company name.

Your company name will show along with your Solution name on your Solution page to potential buyers.

Catalogue Authority/later Public

Supplier registration

Company DUNS

This is in Bravo. This will be used to validate your organisation.

Catalogue Authority

Supplier registration

List of names & emails to authenticate

This is in Bravo. You will be asked to include the names and emails of individuals at your organisation who should have access to the Buying Catalogue under your Supplier organisation account.

Catalogue Authority

Solution details

Solution name

The official name of your Solution. This is not editable once you complete stage 1 Solution details. It should be unique for each Solution. (60 characters max)

Catalogue Authority/later public

Solution details

Solution description

A brief description of your Solution. This information will only be visible to the Catalogue Authority, at this stage. You can edit it in stage 4 before making your Solution page visible to buyers. When it is visible to buyers, it may be shown in search results but will not affect search ranking. (300 characters max)

Catalogue Authority/later public

Solution details

Version (optional)

The current major version number of your Solution if applicable. This is not editable once you complete stage 1 Solution details. 

Catalogue Authority/later public

Solution details

Lead contact

The lead contact is responsible for ensuring the accuracy of information provided and is the Catalogue Authority’s primary point of contact at your organisation as relates to the particular Solution. This contact should be able to resolve or coordinate the resolution of any issues that arise regarding your submission.

This contact will receive all the email notifications relating to the Solution. (You may use a generic email address if notifications should be accessible by multiple users).

Catalogue Authority

Solution details

Additional contacts (optional)

You may add additional contacts as relevant to the Solution. For example, you may wish to provide an additional contact in case your lead contact cannot be reached; Or, you may wish to name a Clinical Safety Officer, or other key contact, for the Solution. These contacts will not be shared outside NHS Digital.

Catalogue Authority

Solution details


You will select the Capabilities that your Solution provides. You can also review the Standards that will be required based on your selections. In selecting each Capability, you will be acknowledging the set of Standards your Solution must meet to attain compliance. You can also review the overarching Standards, with which all Solutions must comply.

In the next stage, your Solution will be assessed against the Capabilities selected.


Capability assessment

Capability assessment evidence method

For each Capability, you can choose to provide evidence either by:

• Providing a recorded video demonstration

• Scheduling a live witness demo

Either way, you will need to demonstrate how each Capability meets its required Epics. (See Confluence for Capabilities and Epics.)

Catalogue Authority

Capability assessment

Video file (conditionally required)

When you provide a recorded video demonstration as evidence, you will need to upload the video file. Video files can be in any video format. If you wish to provide multiple files for each Capability, you must zip them into one file.

Catalogue Authority

Capability assessment

Video timestamps (conditionally required)

For each Capability where you chose to provide a recorded video demonstration, you will need to provide a timestamp indicating where in each video each epic is demonstrated.

Catalogue Authority

Standards compliance

Completed TM files

A Traceability Matrix (TM) will need to be completed for each applicable Standard. TMs are presented as Excel files with a line for each requirement. If you’ve submitted evidence previously for this Solution and Standard, your previously submitted information will be pre-populated, so you’ll just need to fill the gaps. You may include screenshots and other supporting evidence with your submission.

There are further instructions in the TM File.

Catalogue Authority

Standards compliance

Message (optional)

When you submit a TM, you may include a message to the Catalogue Authority if you wish.

Catalogue Authority

The following Build Solution page fields and sections are not confirmed. This stage of the Catalogue is still in development. Therefore, these are subject to change. We will update this table as needed.

Stage Field or Section Description Visibility

Build Solution page

Solution name

The official name of your Solution. This will be brought through from stage 1. It will not be editable.


Build Solution page

Solution version (if provided)

The current major version number of your Solution. This will be brought through from stage 1. It will not be editable.  


Build Solution page

Supplier name

Name of the Supplier organisation you are registered to. It will not be editable.


Build Solution page

Solution description

A brief description of your Solution, which has been pulled through from stage 1. You can edit this field before submitting the page for moderation. (300 characters max)


Build Solution page

Features (optional)

This is a bulleted list. You can add up to 10 bullets to describe a Solution's features.


Build Solution page

List of Capabilities met

List of Capabilities met including epics matched. This will be brought through from Capability assessment. This list is not editable.


Build Solution page

List of Standards met

List of Standards met. This will be brought through from Standards compliance. This list is not editable.


Build Solution page

Catalogue Solution price

This will be based on the relevant framework. It will be populated by the Catalogue Authority and will not be editable.


Build Solution page


Once your Solution has qualified to be on a framework, it will be able to be purchased under that framework. The name of the eligible active framework(s) will display. This field is not editable.


Build Solution page

Service level information

You will have proposed these service levels as part of the Solution submission. The Catalogue Authority will add the relevant information and this will not be editable.

For other types of Solutions, this will be the minimum proposed by the Supplier. (More information on the two types to come)


Build Solution page

Additional Services with prices (optional)

These are services that augment a Solution and are optional for purchase. The prices will be based on the relevant framework. The Catalogue Authority will add the relevant information and this will not be editable.


Build Solution page

Associated Services with prices (optional)

These are services that must or may be purchased with the Solution. The prices will be based on the relevant framework. The Catalogue Authority will add the relevant information and this will not be editable.


Build Solution page


The Catalogue Authority will populate proven integrations, such as IM1 and GPConnect, and the Supplier may add their own proprietary integrations.


Build Solution page

Minimum system requirements

Guidelines for buyers as to what is required to operate the Solution.


Build Solution page

Deployment model and specifications

Guidelines for buyers as to how the Solution is hosted and deployed, including any configurations or requirements to support local deployments.


Build Solution page

About the Solution

You may add more information about your Solution, including contextual links to your website.


Build Solution page

About the Supplier

Free text field about your company, including link to your website.


Build Solution page

Contact details

You may include a name, email and phone number for potential buyers to contact you directly.