Change Management Process and Roadmap Introduction
Introduction
This document provides further information in support of the Change Management and Roadmap Content ancillary document and should be read in conjunction with that and the relevant parts of the Catalogue Agreement.
The ancillary document describes:
- the Capabilities and Standards Model within the operation of the Catalogue Agreement
- the nature of Catalogue changes and the Roadmap
- the manner in which changes will be made to the Roadmap
- the management of Urgent Change within the Catalogue
- the provisions associated with Managed Capacity
- Opportunity Items and associated change.
This page sets out additional detail which builds on these descriptions, in particular regarding the information to be included on the Roadmap, versioning of Standards and Capabilities and the processes of the Catalogue Authority in managing change.
Change Management
Definitions
Term | Definition |
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Horizon | Changes which are on the Horizon will be represented in a separate section of the Roadmap and are included for information purposes. A Horizon item is a potential change which NHS Digital are aware of, but it has either not been formally submitted into the change process and/or is only an idea or high level concept with little or no specification in place. It indicates items which are further into the future and for which it is yet to be determined whether it will progress and if so which of the change routes it will progress through. |
Managed Capacity | The main route for progressing new and uplifted Standards which apply to all relevant Suppliers and which are likely to have a Published specification. Where these have an Effective Date, all relevant Suppliers will be obliged to have achieved compliance with these items by the given date as per the terms of the Catalogue Agreement. Changes in this route will fall into one of four categories:
These items will only be commissioned via the Roadmap and Suppliers are expected to incorporate any development cost within their List Price. Some items in Managed Capacity may be associated with incentive payments for delivery of the change within a certain time boundary. |
Opportunity Item | Opportunities for Suppliers to engage with NHS Digital and the change requestor to collaborate on the definition of specifications and to deliver certain changes early ahead of publication to the wider market where applicable. These will be commissioned via the most appropriate Framework or Procurement vehicle in current operation. Changes in this route will fall into one of two categories:
|
Feasibility Assessment | Opportunities for Suppliers to collaborate with NHS Digital and/or the change requestor to provide information and analysis to assess the feasibility of a new change request before it progresses through another route. These may be either optional or mandatory for Suppliers depending on the nature of the assessment required. |
Urgent Change | Change requests which impact Standards and Capabilities which need to be progressed quickly outside of the usual change management principles. These will account for only a highly restricted volume of change meeting one of two criteria:
|
Draft | This is the status associated with specifications for a new or uplifted Capability or Standard which are still going through definition and elaboration with stakeholders.
At Draft status there will be a Supplier facing Roadmap page on which detail of the specification is released as it becomes available. |
Published | This is the status associated with specifications for a new or uplifted Capability or Standard which are fully defined, agreed and signed off and are not expected to change. Where there is a need for minor or patch uplift, this will be handled as described in the Versioning section. Suppliers would be expected to be working towards achieving compliance with a specification when it is given this status. There may be some Standards and Capabilities which do not progress beyond this status in which case they would be advisory or reflect some other scenario where it remains optional at that point. A checklist will be in place to ensure that before this status is awarded, the specification is adequately defined and ready for implementation with all necessary assurance, implementation and guidance documentation in place to enable a Supplier to complete development at minimal risk. At this point a full version of the Confluence page will be released. In the case of uplifts to existing Standards and Capabilities, this will be a complete, refreshed version of the page e.g. if there is an uplift to Data Standards, the changes will be on or linked to from the relevant Roadmap page and are likely to only show the specific requirements which are changing until it is Published, when a full updated version of the Data Standards page with a revised version number will be made available and will sit alongside the Effective version. |
Effective | This is the status associated with Standards with which all relevant Suppliers are required to have achieved compliance. It is the status associated with Capabilities which have been included within the scope of a Framework request and hence which Suppliers are able to onboard Solutions against and sell via a Framework. When the Effective Date is reached, the old Effective page will be replaced by the new one with an uplifted version number. The old one will be given a status of Retired and moved to an alternate location on Confluence. |
All relevant Suppliers | Suppliers have the choice as to which Capabilities they choose to offer through the Catalogue and as such there are different Standards with which they will need to be compliant. Therefore if a change to a Standard is not applicable to the products and Capabilities the Supplier is offering, then that change is not relevant to them. The Roadmap will indicate the Capabilities and Standards which will be impacted by a particular item on the Roadmap. |
Achieved compliance | This means that a Supplier has been awarded a DevMAC for the Roadmap item. |
Effective Date | The date on which the Standard or Capability becomes Effective. It is the date by which all relevant Suppliers will need to have achieved compliance with the change item. Effective Dates only apply to changes in the Managed Capacity and Urgent Change routes. Some items in the Managed Capacity route may not have an Effective Date, but may be associated with incentive payments for delivery over a certain time period. Those items which do have an Effective Date are mandated for delivery by all relevant Suppliers. |
Backstop Date | This term means the same as Effective Date and should not be used. |
Retired | This is the status associated with old versions of a Capability or Standard which have been uplifted or replaced. These pages may be superseded by a new Published or Effective specification. These pages will remain available for reference in an alternate location on Confluence. |
Deprecated | This is the status associated with Capabilities or Standards which are not yet Retired because products are in live service and still need to be supported. Those Suppliers with pre-existing compliance must maintain this, those with no compliance are not obligated to comply with these Standards. |
Closed | This is the status associated with a change request which will not be progressing. It is recognised that some change requests are submitted into the process and then are not taken forward at some point for a variety of reasons, therefore this status will be used to indicate to Suppliers that a change which had previously appeared on the Roadmap is now no longer required and they should not continue work on it. Changes at this status will remain on the Roadmap for a period of time to ensure awareness. |
Mandated | This term describes a Standard within the Managed Capacity route which Suppliers must deliver and which has been given an Effective Date by which all relevant Suppliers must have achieved compliance. Use of this term should be avoided where possible, instead referring to the Effective Date. |
Incentive item | The term Incentive Item or other terms regarding incentive payments and incentivisation refer to additional funding which may be associated with particular items on the Roadmap. These may be available and applied at the discretion of the Framework and Catalogue Authority and could be applied based on Suppliers maintaining compliance with Effective Dates, for delivery of a change ahead of an Effective Date, or for delivery of items which do not have an Effective Date over a certain bounded time period. |
Versioning | This is defined in the Versioning section |
Roadmap | The Digital Care Services Roadmap, known simply as 'the Roadmap', serves two primary purposes:
|
Priority Standard | This term is used to identify those changes to Standards and Capabilities which have been identified by the NHS England SROs group as the most important and top priority items for the forthcoming period. The Priority Standards may progress through any of the defined change routes, but once in the Managed Capacity route will have an Effective Date. Wherever possible, these items and the associated Effective Dates will be issued for Supplier feedback and agreed in advance of a Framework opportunity such that Suppliers are aware of their obligations and can price accordingly. |
Feature | A change which does not impact a Standard or Capability. |
Lifecycle of Standards and Capabilities
All Standards and Capabilities will go through a lifecycle of Draft to Published to Effective and therefore at any given time (represented by "Day 'X'" on the diagram below) there will be a set of Draft specifications, a set of Published specifications and a set of Effective specifications. The diagram below represents this.
If and when a Standard or Capability is replaced or superseded, it will be given a status of 'Retired' and moved to a new area of Confluence such that it is clear that it is no longer current.
Definitions of Draft, Published, Effective and Retired are included in the table above.
Principles
This section describes a set of principles governing the assessment, management and commissioning of changes to Standards and Capabilities and the Roadmap. The approach to managing change requests which is being adopted by Digital Care Services includes the following:
- A single gated point of entry point for all change requests relating to Digital Care Services Solutions in order that Suppliers should only receive requests for system change from a single source
- A fair, objective and consistent approach to assessing change requests which includes a balanced and comprehensive set of assessment criteria
- A more flexible approach to elaboration, commissioning and delivery of change supported by appropriate commercial mechanisms
- Splitting up larger work items into smaller deliverables to ensure that capacity is not wiped out by a single large initiative
- More opportunities for innovation and collaboration
- More opportunities for the wider market to reduce burden on Suppliers with a greater market share
- Ensuring that Suppliers and wider stakeholders are engaged throughout the change process
- Ensuring that change relating to key strategic priorities and objectives for the wider NHS is delivered in a timely manner
- A Standards and Capabilities Roadmap which presents a single overarching view of all changes which need to be delivered and the opportunities available to Suppliers
- Consultative governance forums and arrangements to ensure Suppliers are fully engaged in the process, are aware of their ongoing obligations and have the opportunity to support the shaping of wider strategy and process improvement
Standards
Draft and Published Standards may be associated with an Effective Date by which all relevant Suppliers are required to have achieved compliance.
Where a Standard is Published but does not have an Effective Date, Suppliers can choose to implement this as a way to differentiate their product and gain market advantage in advance of any Effective Date which may subsequently be set. These items are included on the Roadmap as they would bring benefits to end users and the wider NHS if implemented, but do not currently fall within the key strategic priorities. Any given Framework Authority or Agreement may however choose to incentivise compliance.
NHS Digital will generally aim to agree and set the Standards which are to become Effective during the life-cycle of a Framework in advance of that Framework in order that Suppliers can plan and account for any required development capacity and cost within the List Price to be set at the start of any Framework.
New and uplifted Standards to be progressed through the Urgent Change or Opportunity Items route may be added to the Roadmap at any time. There are however restrictions regarding the addition of new Roadmap entries in the Managed Capacity route where an Effective Date is set. Refer to the Change Management and Roadmap Content ancillary document for this information.
Capabilities
New and uplifted Capabilities may be added to the Roadmap at any time as Draft or Published such that Suppliers could develop against it and begin onboarding. However where this is a material change to an existing Capability or the addition of a new Capability, then this cannot become Effective until a subsequent Framework opportunity. Although in some cases it is likely that the change could be progressed as an Opportunity Item to facilitate quicker delivery prior to a Framework request.
Given that many Capabilities have linked Standards, when a Standard is to be introduced or uplifted as the result of a change request, an assessment will need to be undertaken to determine if the change to the Standard has a significant impact on the scope of the Capability and hence when it can become Effective. This is known as the Materiality assessment and the details of this are set out below.
Routes of change
There are three key routes by which change will be progressed and commissioned following assessment, as shown by the diagram. In addition to these key routes of change, Suppliers will be required to respond to RFIs as per the terms of the Catalogue Agreement, may participate in Feasibility Assessments which will be commissioned via the most appropriate Framework or procurement vehicle and may also initiate change themselves based on internal development and delivery plans. It is possible that these routes may be used in parallel or consecutively for a single change. For example there may be a change request which is a standalone feature or perhaps a new messaging interface specification which is best progressed initially as an Opportunity Item, before being Published and given an Effective Date for development and implementation by all relevant Suppliers via the Managed Capacity route. A Feasibility Assessment may be used to engage Suppliers as part of elaborating a specification and/or to understand the parameters of a change prior to it progressing into one of the other change routes.
Managed Capacity
Changes progressing through this route are published for all relevant Suppliers to deliver i.e. the new or uplifted Standard may or may not apply dependent on the Capabilities which a Supplier has selected to support. Suppliers are expected to incorporate the cost of the capacity required to deliver items in the Managed Capacity route which have an Effective Date within the life-cycle of the Framework as part of their List Price set for that Framework. Suppliers must ensure that they make available sufficient capacity to deliver all the work specified via the Standards and Capabilities Roadmap which falls within the life-cycle of the applicable Framework. Capacity issues shall not relieve a Supplier of their obligations to achieve compliance with the relevant Standards by the set Effective Dates.
It is anticipated that the majority of changes in the Managed Capacity route which have an Effective Date within the life-cycle of the subsequent Framework will be discussed and agreed with Suppliers ahead of that Framework in order that Suppliers can set their List Price accordingly. However the Catalogue Authority reserves the right to add items to the Roadmap within the life-cycle of a Framework which will also become Effective during that Framework. Given that the Frameworks are expected to be relatively short, this is not expected to be a common scenario as any given Effective Date is likely to fall within a subsequent Framework, thus allowing a Supplier to re-set their List Price, however any such occurrence will be handled as per the terms set out in the Change Management and Roadmap Content ancillary document. It should also be noted that the Catalogue Agreement does not restrict the ad hoc resetting of the List Price subject to the conditions set out in the Commercial Standard and the Framework Agreement.
There will be four categories of change item within Managed Capacity:
- The key strategic (SRO Priority) changes, as agreed by the NHS England CCIO with the support of the Senior Responsible Owners (SRO) group which will need to be implemented by a set Effective Date within the life-cycle of the Framework. This is the group who are accountable for the prioritisation and delivery of the key Department of Health and Social Care and NHS England strategies and objectives (e.g. Secretary of State Technology Vision). These items will generally be agreed with Suppliers ahead of any Framework opportunity and should be accounted for in the List Price set for the Framework.
- Regulatory and legislative change which must be delivered by a set Effective Date. These items should be accounted for in the List Price set for the Framework.
- Minor and Patch uplifts to previously Published or Effective specifications which will be regular items on the Roadmap to account for small tweaks to existing specifications with Effective Dates every three months. These could include minor or patch uplifts to a range of Standards or Capabilities but the volume of change in each entry will be carefully monitored. It is anticipated that these uplifted specifications would be published a minimum of three months in advance of each Effective Date. As per the Change Management and Roadmap Content ancillary document, these items should be accounted for in the List Price set for the Framework.
- A list of other changes which deliver benefits to the NHS and which NHS Digital would like to be delivered. These items will have Published specifications and may or may not have Effective Dates. These items should not be accounted for in the List Price set for the Framework, however they may be associated with incentive payments for delivery of the change item within a particular bounded time period.
- For example - the introduction of a new version of the Electronic Prescribing Service (EPS). Plans could be issued by the NHS Digital spine team to retire old versions across the market in four years. The new specification which introduces a change to the existing EPS Standard could be Published alongside the Effective specification. Suppliers are then able to implement either the new Published version or the existing Effective one and both would be deemed as compliant. However, closer to the retirement date of the existing Effective specification (perhaps two and a half years in), an Effective Date by which Suppliers will need to have achieved compliance may then be set for the new Standard. Therefore until that point there will be a Published Standard which is not Effective.
- For example - the introduction of a new version of the Electronic Prescribing Service (EPS). Plans could be issued by the NHS Digital spine team to retire old versions across the market in four years. The new specification which introduces a change to the existing EPS Standard could be Published alongside the Effective specification. Suppliers are then able to implement either the new Published version or the existing Effective one and both would be deemed as compliant. However, closer to the retirement date of the existing Effective specification (perhaps two and a half years in), an Effective Date by which Suppliers will need to have achieved compliance may then be set for the new Standard. Therefore until that point there will be a Published Standard which is not Effective.
When items in the Managed Capacity route are given an Effective Date, they become mandatory. Effective Dates will be objectively justified for the purpose of transparency and will determine the date by which all relevant Suppliers are required to have achieved compliance. The Effective Date will be set in conjunction with Suppliers as far as is reasonably practicable, however for some changes, especially those related to regulatory or legislative change, this may not be possible. Where a Supplier considers that it is unreasonable for them to achieve a given Effective Date, they must notify the Catalogue Authority as soon as is reasonably practicable. Suppliers will have the right to raise disputes in relation to any Effective Date which they consider to be unattainable with regard to the scope or complexity of the work item but valid reasoning will need to be provided.
Suppliers will generally be able to select and develop items in the Managed Capacity route in a manner to suit their development plans and approach, but must ensure that they deliver all the key strategic priorities identified by the NHS England SRO group and achieve compliance by the set Effective Dates. As per the Change Management and Roadmap Content ancillary document, Suppliers are expected to work with the Catalogue Authority to share and agree delivery plans and development milestones to ensure that obligations can be met.
All changes in the Managed Capacity route will appear on the Roadmap and will not be commissioned via a separate mechanism. The Roadmap will clearly display which of the four categories the item is in, the Effective Date and the availability of incentives where applicable.
Opportunity Items
Supplier capacity for participation in items in this route is in addition to any capacity or pricing assigned to changes in the Managed Capacity route. Additional funding may be made available for Opportunity Items. Changes progressing through this route will offer Suppliers the opportunity to develop and deliver certain changes early and ahead of the wider market (where applicable), to 'get ahead of the game' and increase the marketability of their products or allow for them to move into new markets and offer additional products and services through the Framework. These opportunities will be commissioned via the most appropriate Framework or procurement vehicle in current operation at the time and the parameters of each particular Opportunity Item, such as outcomes/outputs, timescales, any associated funding and which Suppliers will be eligible, will be determined on a case by case basis. There are two types of item in this route:
Alpha, Definition and First of Type (see the Change Management and Roadmap Content ancillary document). Opportunities for Suppliers to collaborate and co-produce specifications and to develop these up to the First of Type stage and to refine the specification before it is Published for all other relevant Suppliers to implement through the Managed Capacity route.
Other opportunities (see the Change Management and Roadmap Content ancillary document). Opportunities for the wider Supplier market to deliver changes such as new Capabilities or standalone features which do not necessarily have to be implemented by Foundation Solution Suppliers or Suppliers supporting a particular Capability. These opportunities may allow a Supplier to set their product apart from others and potentially enter new markets and gain market share or offer a product via the Framework which they may have not been able to previously. These are changes which may be more efficiently and effectively delivered by Suppliers who already have existing products to meet the desired business needs rather than commissioning bespoke development from existing Suppliers.
Feasibility Assessment
(See the Change Management and Roadmap Content ancillary document). The Feasibility Assessment process will be controlled in the same manner as the Opportunity Items. It is to cover change requests requiring an assessment involving input, analysis and feedback from Suppliers to assist in determining the feasibility, scope, sizing/complexity and nature of the change request prior to it progressing through one of the other change routes and also to assist in defining specifications. This is for work which does not require any development, but goes beyond the scope and time required for an RFI as set out in the Catalogue Agreement. Following completion of the Feasibility Assessment, the change may either be withdrawn or progressed via one of the other change routes.
Urgent Change
Please refer to the Change Management and Roadmap Content ancillary document for information regarding Urgent Change.
RFI / Analysis only
Please refer to the Catalogue Agreement
Supplier Initiated Change
Supplier initiated changes are included on the diagram to reflect the fact that Suppliers have their own internal plans and roadmaps for product development and delivery which also require capacity and their own release cycles. These will be handled as per the relevant Service Management and Commercial Standards and Schedules.
Supplier obligations
As per the Change Management and Roadmap Content ancillary document, Suppliers are obliged to share their Delivery Plans in relation to items on the Roadmap with the Catalogue Authority to facilitate alignment of work items between these plans and the Standards and Capabilities Roadmap. This should include as a minimum:
- detail of which items they are currently working on
- target delivery and implementation dates
- any risks or challenges in meeting Effective Dates set
- information regarding which items they intend to develop next
- information regarding which Opportunity Items they intend to bid for
- some detail regarding alignment to the wider technology strategy of the Supplier and the NHS.
The earlier these plans are made available and the more detail they contain, then the development and delivery of the change should be more efficient and effective enabling the Supplier to meet Effective Dates and achieve incentives where available.
Change Management Process
This section is additional to any information contained within the Change Management and Roadmap Content ancillary document. It describes the proposed processes for managing the request, assessment and commissioning of change within the Authority and the addition of that change to the Roadmap.
The Digital Care Services Change Management process has been set up as a high level overarching process flow shown and explained below, and a series of sub processes which are detailed in the expandable sections beneath. Some of these sub-processes are covered in other documents or are determined on a case by case basis. This is primarily a process internal to NHS Digital, but Suppliers will be involved at various points and it is being shared for transparency as to how change requests will be handled.
The change process is triggered by the submission of a change request to the Digital Care Services Change team, including changes coming out of the Tech Strategy and the ongoing internal review of Standards and Capabilities. The change request process will be open for submissions at any time and changes will be submitted via a standardised form template giving the key information required regarding the change.
The change assessment process will analyse the details and background of the request to determine the most efficient and effective route for it to be progressed. It is made up of two key aspects:
- Entry Assessment. An internal assessment of the fundamental details and reasons behind the change request and consideration of the validity and necessity of the change to determine whether it should be progressed and added to the Roadmap. The intention of this stage is to filter out any requests which are not deemed to be necessary, are already in train with other work requests or which are not in a sufficient state of readiness to be progressed, such that Suppliers and other key stakeholders are not engaged in the work unnecessarily.
- Full Assessment. Analysis of the finer detail of the change request to consider the most appropriate change route and set the parameters for delivery and how the change will be commissioned.
Further definition of these stages is included in the processes below. There are three main outcomes following these initial assessments, although they may need to be repeated to refine the details of the request prior to a final decision being made:
- Rejected. Determined by the assessment team that the change should not be progressed. This may mean it is covered by or merged with other work, the request is not ready to be progressed or that it is in some way not suitable for the Digital Care Services change process i.e. it is not relevant to the current scope of Digital Care Services or may be better progressed via an alternate mechanism
- Withdrawn. Change requestor opts to withdraw the change following assessment and feedback
- Added to the Roadmap and assigned to a change route
- RFI and/or Feasibility Assessment
- Urgent Change
- Opportunity Item
- Managed Capacity
Rejected or Withdrawn end the change process for that submission, although it is expected that some of these changes may be resubmitted into the process down the line. Adding the change to the Roadmap triggers further processes which are detailed below.
Entry Assessment
Full Assessment
Managed Capacity
Opportunity Item
Urgent Change
Standards and Capabilities Versioning
As per Section 1 of this document, all Capabilities and Standards will have a version number. These version numbers will be in the format "a.b.c", where:
- a = major version
- b = minor version
- c = patch version
Some key principles regarding these version numbers are set out below:
- When a major version number is updated, the equivalent minor and patch version numbers will be reset to zero (e.g. 2.1.2 becomes 3.0.0)
- Version numbers for Capabilities and Standards are independent of any Framework and will therefore carry over if no updates are to be made between Frameworks
- Capabilities and Standards (including Capability Specific Standards) will have separate version numbers which will be iterated independently i.e. if the Prescribing Standard moves from v1.0.0 to v1.1.0, this does not always mean that the version number of the Prescribing Capability will also change.
- Any time a change is introduced which impacts an existing Capability and/or Standard, the version number will be iterated.
- The iteration of version numbers only applies to changes which impact an existing specification. Specifications for new Capabilities and Standards will always be major changes and will always be set at version 1.0.0 when initially Published.
Definitions
The definitions of major, minor and patch and how it would be determined as to whether a particular change requires a major, minor or patch change to the version number are detailed below. It should be noted that there is not necessarily a 'one size fits all' definition of these terms as what applies to an API for example would likely be very different to what applies to the Epics and Acceptance Criteria which make up a Capability. Therefore these definitions have been deliberately left fairly broad and they would be assessed accordingly as part of the change process. In the case of changes to APIs, these have been based around https://semver.org/.
Major: Change has a material impact on Capability or Standard and Suppliers will need to update their Solutions to remain compliant AND/OR a version when breaking or incompatible (i.e. not backwards compatible) changes are made.
Minor: Change does not have a material impact on Capability or Standard, but indicates a Supplier may need or wish to update their Solution AND/OR a version when larger non-breaking changes or a significant number of smaller non-breaking (i.e. backwards compatible) changes are made; or an unsubstantive breaking change is made.
Patch: Change does not have a material impact on Capability or Standard and minimal or no update to Supplier Solutions is required such as the introduction of additional guidance or clarifications, correction of grammatical errors or typos, restructure or reformatting of requirements AND/OR a version when smaller non-breaking changes or backwards compatible bug fixes are made.
How will version uplifts be handled through the Change process?
All changes entering the Change Management Process will be assessed to determine whether they are a patch, minor or major uplift to a specification and the parameters of the change and Effective Dates will be set accordingly as per the processes set out above.
There may be scenarios where a specification which has been Published in the Managed Capacity route and given an Effective Date needs to be amended for some reason and changes what a Supplier is required to deliver, or may already have delivered. It is hoped that this will not be a common scenario, although it is more likely to apply to some things (e.g. APIs and messaging specifications) than others. The following mechanisms and principles will be used to manage this:
Major changes: Any revisions which are assessed as major changes will be assessed through the Change Management Process and the Effective Dates and other parameters associated with the change adjusted accordingly to account for the work required from Suppliers. The Roadmap would be updated as necessary to reflect this change and this may be subject to the restrictions set out in the Change Management and Roadmap Content ancillary document.
Minor or patch changes: There will be items on the Roadmap in the Managed Capacity route with Effective Dates every three months to cover minor and patch uplifts to a range of existing specifications which are either Effective or Published. For example, each entry on the Roadmap could cover possible uplifts to GP Connect interfaces, IM1, GP2GP or other APIs or messaging specifications etc. but there would not be an uplift to all of these within each and every entry on the Roadmap. The scope of what is included within these will be carefully managed and monitored. Suppliers will be expected to allow capacity for these items within their List Price.
Taking this approach sets a regular rhythm for Suppliers in keeping up to date with the latest versions of specifications and allowing them to plan for this, but also for Programmes in managing their specifications and knowing when they can release patch or minor uplifts and when they can expect that they will be developed. It is expected that the details of what is to be included in each 3 monthly Roadmap entry and the specifications will be published a minimum of 3 months ahead of each Effective Date.
Digital Care Services Standards and Capabilities Roadmap
The Digital Care Services Roadmap ('the Roadmap') will provide a single, summary view of all the changes and opportunities for Suppliers regarding new and uplifted Standards and Capabilities, whichever route they are to be progressed through. This may include 'Horizon' items which Digital Care Services are aware of and are expecting to be progressed via the defined change routes at some point further into the future, but which have not yet been formally requested and may not materialise. The Roadmap will be the only mechanism by which changes in the Managed Capacity route will be commissioned. Changes following other routes will be commissioned via separate mechanisms as described in the Change Management and Roadmap Content ancillary document, but will still be displayed on the Roadmap. .
What information will be shown on the Roadmap?
The Roadmap will include a summary of information to ensure Suppliers are fully aware of the changes that are required and the opportunities which are available to them. Some of the data items are common to all change routes, and other data items are specific to a particular change route. The table below sets out the information to be included. Horizon items are not included in this table as they will not have been assigned to a change route and there is likely to be limited information available about the change. Dependent on the final form presentation of the Roadmap, certain information, such as the change route, may not be given in distinct fields and may instead be represented in an alternate format, such as in labelled swim lanes or with colour coding or sections.
Field name | Field content |
---|---|
Title | A unique name for the change |
Description | A very brief summary of the change |
Date added | The date the item was added to the Roadmap |
Type | All Roadmap entries will be set to a type of 'Roadmap' NB. Once the change specification is Published, the equivalent field on the page for the Published specification will be updated to one of the other options (i.e. Overarching, Interoperability, Capability Specific, Context Specific) to reflect the type of entity the change relates to e.g. if it is a change to the Prescribing Standard, this entry would then become 'Capability Specific Standard' |
Standards/Capabilities | List of the existing Standards and/or Capabilities which are impacted by the change |
Change Route | Which of the designated change routes the item is going through or Horizon if not yet determined. Options for:
NB. This is likely to be represented in a different format on the Roadmap view rather than in a separate field |
Change Type | An indication as to the type of change this is:
|
Status | The status of the change item, which also includes the status of the specification within that. Options to be:
NB. This field will be marked as 'n/a' for Horizon items. There will only be one Status entry for each Roadmap item |
Effective Date | The Effective Date of the change NB. This will not be set for some items in Managed Capacity and does not apply to Opportunity Items or Horizon |
Incentives / Funding | An indication of whether additional incentives or funding will be available for this change |
Incentive Dates | The dates during which the incentive applies |
ID | A unique ID for the Roadmap entry in the format "RMXX" NB. Once the change specification is Published, the equivalent field on the page for the Published specification will be updated to reflect the type of entity that this is e.g. if it is a change to the Prescribing Standard, this entry would become 'S14' ; if this is a new or replace item, then a new ID in the same format will be created. |
Version | The version number of the Roadmap entry in the format a.b.c to indicate when changes have been made to the Roadmap entry, such as a new draft specification being issued or an amendment to one of the parameters associated with the change. NB. Once the change specification is Published, the equivalent field on the page for the Published specification will be updated in alignment with the version number of the Standard or Capability which is being uplifted or be set to 1.0.0 if this is a new or replace item. |
In addition to the Roadmap, each Capability and Standard on Confluence contains a Roadmap section linking to a page which details any Roadmap items related to that Capability or Standard and the details of that change. There is also a central Roadmap page on Confluence where a full list of Roadmap items will be available with a summary of information similar to the above.
Roadmap Content
The Roadmap area of Confluence presents the details of the items on the Roadmap.