Off-Patent Biologicals and Biosimilars Tendering in Europe-A Proposal towards More Sustainable Practices

Background: In Europe, off-patent biologicals and biosimilars are largely procured by means of tender procedures. The organization and design of tenders may play a key role in the evolving biosimilar market, and currently, it is not fully elucidated how tenders for off-patent biologicals and biosimi...

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Main Authors: Liese Barbier (Author), Steven Simoens (Author), Caroline Soontjens (Author), Barbara Claus (Author), Arnold G. Vulto (Author), Isabelle Huys (Author)
Format: Book
Published: MDPI AG, 2021-05-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Liese Barbier  |e author 
700 1 0 |a Steven Simoens  |e author 
700 1 0 |a Caroline Soontjens  |e author 
700 1 0 |a Barbara Claus  |e author 
700 1 0 |a Arnold G. Vulto  |e author 
700 1 0 |a Isabelle Huys  |e author 
245 0 0 |a Off-Patent Biologicals and Biosimilars Tendering in Europe-A Proposal towards More Sustainable Practices 
260 |b MDPI AG,   |c 2021-05-01T00:00:00Z. 
500 |a 10.3390/ph14060499 
500 |a 1424-8247 
520 |a Background: In Europe, off-patent biologicals and biosimilars are largely procured by means of tender procedures. The organization and design of tenders may play a key role in the evolving biosimilar market, and currently, it is not fully elucidated how tenders for off-patent biologicals and biosimilars are designed and if approaches are aligned with sustaining market competition and societal savings for healthcare systems over the long term. This study aims to (i) explore the design and implementation of tender procedures for off-patent biologicals and biosimilars in Europe, (ii) identify learnings for sustainable tender approaches from purchasers and suppliers, and (iii) formulate recommendations in support of competitive and sustainable tender practices in the off-patent biologicals market. Methods: A mixed methods design was applied. A quantitative web-survey was conducted with hospital pharmacists and purchasers (N = 60, of which 47 completed the survey in full), and qualitative expert-interviews with purchasers and suppliers (N = 28) were carried out. Results: The web survey results showed that the organization and design of tenders for off-patent biologicals and biosimilars, and the experience of hospital pharmacists and purchasers with this, considerably varies on several elements across European countries. From the qualitative interviews, signals emerged across the board that some of the current tender approaches might negatively affect market dynamics for off-patent biologicals and biosimilars. The focus on generating short-term savings and existence of originator favouring tender practices were identified as elements that may limit timely competition from and market opportunity for biosimilar suppliers. The need to optimize tender processes, considering a more long-term strategic and sustainable view, was expressed. In addition, challenges appear to exist with differentiating between products beyond price, showing the need and opportunity to guide stakeholders with the (appropriate) inclusion of award criteria beyond price. Due to the variety in tender organization in Europe, a 'one size fits all' tendering framework is not possible. However, on an overarching level, it was argued that tender procedures must aim to (i) ensure market plurality and (ii) include award criteria beyond price (warranted that criteria are objectively and transparently defined, scored and competitively rewarded). Depending on the market (maturity), additional actions may be needed. Conclusions: Findings suggest the need to adjust tender procedures for off-patent biologicals and biosimilars, considering a more long-term strategic and market sustainable view. Five main avenues for optimization were identified: (i) safeguarding a transparent, equal opportunity setting for all suppliers with an appropriate use of award criteria; (ii) fostering a timely opening of tender procedures, ensuring on-set competition; (iii) ensuring and stimulating adherence to laws on public procurement; (iv) securing an efficient process, improving plannability and ensuring timely product supply and (v) safeguarding long-term sustainable competition by stimulating market plurality. 
546 |a EN 
690 |a tender 
690 |a procurement 
690 |a off-patent 
690 |a biological 
690 |a biosimilar 
690 |a award criteria 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 14, Iss 6, p 499 (2021) 
787 0 |n https://www.mdpi.com/1424-8247/14/6/499 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/224e1e47e3d54e45a9a29d2a0ec08b9b  |z Connect to this object online.