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IM1 pre requisites form
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IM1 prerequisites
Form submitted successfully
NHS England's IM1 team will be in touch in the near future to confirm next steps.
Section 1: Your details
Name
*
Full name
Email
*
Organisation name
*
Product name
*
Name of the IM1 product you are wanting to onboard with
Section 2: Clinical safety prerequisites
Confirm the following prerequisites are already in place:
A qualified Clinical Safety Officer is in place
*
Yes
A detailed use case description that covers the entirety of the product
*
Yes
A written clinical safety process and a commitment to uplift this as required with the development of the IM1 product
*
Yes
Ability to populate a detailed hazard log template and a commitment to uplift this as required with the development of the IM1 product
*
Yes
Confirm that if the product contains software as a medical device you understand that this would be subject to additional scrutiny
*
Yes
Section 3: Information governance prerequisites
Confirm you are committed to the following:
Starting the process of obtaining a Data Security and Protection Toolkit (DSPT) annual assessment, to be in place by time of go live
*
Yes
Completing a Data Protection Impact Assessment including Transparency/Privacy Notice for the consuming supplier and for associated applications and services as required for relevant use cases
*
Yes
Utilising an Information Security Management System (ISO 27001 recommended)
*
Yes
Completing a penetration test (pen test) which must be completed by a 3rd party CHECK / CREST accredited organisation, prior to go live and annually thereafter. The CHECK / CREST accredited organisation must be accredited to conduct penetration testing
*
Yes
A UK location for processing patient data
*
Yes
Section 4: Provider suppliers
Confirm which provider supplier(s) you would like to integrate with (you may select more than one):
EMIS (EMIS Web)
Yes
TPP (SystmOne)
Yes
Medicus
Yes
Section 5: Use case and benefits
What will you use IM1 access for and how will it improve delivery of care?
*
2000 character limit. Please state the clinical use case and summarise the release scope for the product, including the benefits to the NHS and patient clinical care.
Interface options
EMIS
PFS
Transaction
Partner
Bulk
TPP
PFS
Transaction
Bulk
Other GP new market entrants as when available
Medicus
Other
If 'Other', please name the new market entrant
If using PFS, would you be utilising NHS Login as an authentication method for PFS?
Yes
No
Does your use case use artificial intelligence (AI)?
*
Yes
No
If yes, how?
2000 character limit
Are the following documents to support your application to IM1 in a draft state?
Data Protection impact assessment (DPIA)
*
Yes
No
Clinical safety case
*
Yes
No
Hazard log
*
Yes
No
Medical device status of certification (if applicable)
Yes
No
Please add any other supporting information you feel relevant
2000 character limit