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HTA
This page shows the latest HTA news and features for those working in and with pharma, biotech and healthcare.
NICE wants to stop saying ‘no’ – but needs pharma’s co-operation
However, he cautioned that industry, healthcare payers and health technology assessment (HTA) authorities like NICE needed to do more to achieve ‘alignment’ on value, evidence and price for the sake of
Latest news
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Gene Genie
As that tripartite HTA project suggests, we haven’t figured out how to put. ... Can these very expensive treatments ever be affordable, even if HTAs pronounce them as good value?
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Novartis first to benefit from NICE advice on ‘patient preference’
patients and generate evidence for health technology assessment (HTA).
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NICE and Canadian counterpart to offer joint advice service
Agencies offer parallel scientific advice. NICE and the Canadian Agency for Drugs and Technology in Health (CADTH) have joined forces to offer pharma a health technology assessment (HTA) service. ... The two HTA agencies have many methodologies in
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How to pay for very high cost, curative drugs? ICER and NICE put their heads together
handle. Now three health technology assessment (HTA) organisations are collaborating on how to adapt their cost effectiveness and value for money assessments. ... The collaboration between the HTA bodies reflects similar moves in Europe, where groups of
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Vertex gains EU approval for earlier Orkambi use
on safety and efficacy as measured by changes in sweat chloride levels, However these are not related to changes in lung function, the kind of clinically important data which European HTA
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Approximately 32 fully matching, plus 142 partially matching documents found.
Latest Intelligence
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Digital applications are transforming the market access landscape
The inbuilt case logic is able to identify risks and maximise opportunities at all levels, from assets in preclinical development through to country HTA submissions. ... This facilitates increased collaboration by linking global thinking with affiliate
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Alnylam’s big moment: bringing groundbreaking RNAi drugs to Europe
Alnylam will face a similar process with Europe’s many national HTA organisations.
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Lonely planet: why there is dwindling value in pharma travelling alone
Similarly, in a move away from paternalistic models of healthcare delivery, HTA bodies are beginning to involve patients in assessments to establish and enshrine the factors that matter most to them
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Stakeholder dialogue in Europe’s adaptive pathways pilot
In the scientific advice sessions, involvement was limited to regulators and HTA bodies and, in some instances, clinicians and patients. ... He is a leader in Integrated Scientific Advice, combining HTA, regulatory and patient perspectives, and
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The European Medicines Agency: PRIME’d for access?
There could be some grounds for optimism though: the PRIME scheme includes the option for HTA agencies – and patients – to be involved in giving scientific advice. ... So far, 37 sessions of scientific advice have taken place for 22 products, with
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Approximately 14 fully matching, plus 53 partially matching documents found.
Latest appointments
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Open Access Consulting appoints new director
value dossiers, payer-focused objection handlers, stand-alone payer value propositions and local HTA submissions.
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Claes Buxfeldt joins NDA
He becomes its new HTA director. AstraZeneca’s former global price and reimbursement director Claes Buxfeldt has joined the NDA advisory board. ... Buxfeldt’s new role at NDA will see him drive and develop the group’s service offerings in the HTA
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Professor Carole Longson moves from NICE to the ABPI
She most recently spent the 18 years at the National Institute for Health and Care Excellence ( NICE), where she has led the HTA organisation’s technology appraisal programme.
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VCLS appoints Carole Jones to senior market access role
her focus on expanding the company’s market access capabilities, spanning payer strategy, health economics and outcomes research (HEOR), health technology assessment (HTA) and communications support.
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EFPIA's Richard Torbett to move to the ABPI
At the ABPI Torbett will focus on pricing, the Pharmaceutical Price Regulation Scheme (PPRS), health technology assessments (HTA) and value assessment, as well as market access in the UK.
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Approximately 0 fully matching, plus 7 partially matching documents found.
Latest from PMHub
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Digital applications are transforming the market access landscape
The inbuilt case logic is able to identify risks and maximise opportunities at all levels, from assets in preclinical development through to country HTA submissions. ... This facilitates increased collaboration by linking global thinking with affiliate
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Achieve up to 80% auto-population of your first draft HTA submission
Integrated support from the PRMA Consulting team provided critical analysis of global documents and alignment on country specific HTA strategy. ... The HTA submission that we produced using the PRMA Navigator saved us weeks.
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Video: Drive payer submission readiness for your Phase 2 and 3 products
Accelerates HTA submission readiness by producing a high-quality evidence generation plan driven by informed, collaborative, and integrated decision-making.
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Drive payer submission readiness for your Phase 2 and 3 products
Accelerates HTA submission readiness by producing a high-quality evidence generation plan driven by informed, collaborative, and integrated decision-making.
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PRMA Consulting Ltd
Global reimbursement Director, top-20 pharmaceutical company. “The HTA submissions produced using the PRMA Navigator.
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Approximately 4 fully matching, plus 12 partially matching documents found.
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