New Survey by SFL Regulatory Affairs & Scientific Communication and EuropaBio Highlights Poor Awareness of HTA Among Biotech SMEs in Europe

Published: Mar 27, 2012

March 27, 2012 -- To evaluate new and innovative medical treatments in a more systematic way, governments in Europe are increasingly turning to health technology assessment (HTA).

A survey was conducted by EuropaBio and SFL Regulatory Affairs & Scientific Communication Ltd. (SFL) to evaluate the understanding and approach to HTA of small and medium size enterprises (SMEs) which are involved in drug development. The survey results show that in many cases, European biotech SMEs find it challenging to adjust to the increasing use of HTA as they strive to bring their products to market. SMEs face a number of specific challenges during development and prior to approval and commercialisation, operating under tight financial constraints and with limited human resources. Under these specific constraints, being able to afford the appropriate expertise and to meet additional requirements to fulfil HTA obligations can be an issue. The results from responding SMEs indicate that the general knowledge of HTA requirements and processes is poor among biotech SMEs. Very few companies reported that HTA has had any impact on their clinical trial design or other key decisions during the development stage. The survey also points to a worrying lack of communication between SMEs and HTA authorities.

“There is anecdotal information that SMEs are struggling with HTA.” explains Thomas Bols, Chair of EuropaBio’s Healthcare Council “To address this situation, we needed facts about the nature and extent of the problem. Information from HTA, such as clinical effectiveness and cost effectiveness, is increasingly required by authorities to take decisions on pricing and reimbursement, and allocation of healthcare funding.”

“The low awareness of HTA among biotech SMEs and, as a consequence, the struggle to demonstrate the value of their products, can be a serious problem. If biotech SMEs cannot gain funding, their product may never reach patients, who in turn may miss out on new treatments that could greatly improve their lives” commented Bols.

“This issue is an important one, which EuropaBio will want to address in European fora which discuss HTA issues, such as EUnetHTA project.”

“Most biotech SMEs are drug developers, but currently, all do not possess the expertise to market these products in the face of rigorous demands of HTA. What is needed is a shift in the mind-set of both HTA authorities and SMEs alike which recognises that gathering information for HTA is a shared responsibility. Importantly, we need to see what the EU and HTA bodies, and the biotech industry itself, can do to better support SMEs during this process.” said Anna Hallersten, Public Affairs Director at SFL.

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