In deliveryUnited KingdomGoodsFramework agreement£1,520,432,295
NHS National Framework for Medical Retinal Vascular Treatments - 1 December 2025
- Published
- Published 19 June 2025
- Deadline
- Closed 14 July 2025
Overview
NHS National Framework for Medical Retinal Vascular Treatments - 1 December 2025
Offer reference number: CM/PHS/25/5728
Period of framework agreement: Dates detailed below, with an option or options to extend (at the discretion of the Authority) up to maximum of 24 months.
Potential periods of call-offs under the framework agreement:
CM/PHS/25/5728/01 - National Framework for Medical Retinal Vascular Treatments:
7NAT (National) 01/12/2025 to 31/05/2027 (18 months)
CM/PHS/25/5728/02 - Regional Framework for Medical Retinal Vascular Treatments aflibercept 2mg:
NOFE: (North of England) 01/12/2025 to 31/05/2027 (18 months)
SOFE: (South of England) 01/12/2025 to 31/05/2027 (18 months)
MAE: (Midlands and East) 01/12/2025 to 31/05/2027 (18 months)
LNW: (London) 01/12/2025 to 31/05/2027 (18 months)
Published By: Medicines Procurement and Supply Chain – NHS Medicines Value & Access, NHS England
Provision of Licensed Medical Retinal Vascular Anti Veg-F and Intravitreal Corticosteroid medicines used in medical retinal vascular services for the NHS in England. To include but not limited to aflibercept, bevacizumab, brolucizumab, intravitreal dexamethasone, intravitreal fluocinolone, faricimab and ranibizumab used in the treatment of;
• neovascular (wet) age-related macular degeneration (AMD)
• visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO)
• proliferative diabetic retinopathy (PDR)
• visual impairment due to diabetic macular oedema (DME)
• visual impairment due to diabetic macular oedema (DME) who are pseudophakic or who are considered insufficiently responsive to, or unsuitable for non-corticosteroid therapy
• vision impairment associated with chronic diabetic macular oedema, (DME)
• visual impairment due to myopic choroidal neovascularisation (myopic CNV)
• retinopathy of prematurity (ROP) with zone I (stage 1+, 2+, 3 or 3+), zone II (stage 2+ or 3+) or AP-ROP (aggressive posterior ROP) disease
• inflammation of the posterior segment of the eye presenting as non-infectious uveitis
• prevention of relapse in recurrent non-infectious uveitis affecting the posterior segment of the eye
Key details
- Country
- United Kingdom
- Status
- In delivery
- Category
- Goods
- Estimated value
- £1,520,432,295
- Procedure
- Open
- Contract type
- Framework agreement
- SME suitable
- Yes
- Published
- 19 June 2025
- Questions by
- 7 July 2025
- Deadline
- Closed
Pharmaceutical productsVarious medicinal products
Award outcome
- Awarded value
- £2,254,670,118
- Award date
- 30 July 2025
- Contract period
- 1 December 2025 → 31 May 2027
- ABBVIE LTD
- ALIMERA SCIENCES LIMITED
- Abbvie Ltd
- Alimera Sciences
- BAYER PUBLIC LIMITED COMPANY
- BIOGEN IDEC LIMITED
- BIOSIMILAR COLLABORATIONS IRELAND LIMITED
- Bayer Plc
- Biogen
- Biosimilar Collaborations Ireland Limited
- CELLTRION HEALTHCARE UNITED KINGDOM LIMITED
- Celltrion Healthcare United Kingdom Limited
- MDBIOLOGICS LTD
- NOVARTIS PHARMACEUTICALS UK LIMITED
- Novartis Pharmaceuticals UK Ltd
- ORION PHARMA (UK) LIMITED
- Orion Pharma (UK) Ltd
- Outlook Therapeutics, Inc.
- ROCHE PRODUCTS LIMITED
- Roche Products Ltd
- SANDOZ LIMITED
- TEVA UK LIMITED
- THORNTON & ROSS LIMITED
- Teva UK Limited
- Thornton and Ross Ltd
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Notice history
Every published notice in this contracting process, newest first.
Contract
6 October 2025
View notice ↗Contract
1 August 2025
View notice ↗Tender Update
19 June 2025
View notice ↗Contract Notice
19 June 2025
View notice ↗
Contracting authority
NHS ENGLAND
BuyerLeeds, United Kingdom
GB-NHS: X24
NHS England
BuyerLondon, United Kingdom
GB-PPON: PDPT-3135-BWWY
Authority website ↗
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