-
Americas
-
Asia & Oceania
-
A-I
J-Z
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Regions
-
Americas
-
Asia & Oceania
-
Europe
-
Middle East & Africa
-
Americas
-
Asia & Oceania
-
Europe
Europe
- Adriatic
- Belgium
- Bulgaria
- Czech Republic
- Deutschland
- España
- France
- Greece
- Hungary
- Ireland
- Israel
- Italia
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
SOLUTIONS
-
Research & Development
-
Real World Evidence
-
Commercialization
-
Safety & Regulatory Compliance
-
Technologies
LIFE SCIENCE SEGMENTS
HEALTHCARE SEGMENTS
- Information Partner Services
- Financial Institutions
- Public Health and Government
- Patient Associations
- Payers
- Providers
THERAPEUTIC AREAS
- Cardiovascular
- Cell and Gene Therapy
- Central Nervous System
- GI & Hepatology
- Infectious Diseases and Vaccines
- Oncology
- Pediatrics
- Rare Diseases
- View All
Impacting People's Lives
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
LEARN MORE
Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
Research & Development OverviewResearch & Development Quick Links
Real World Evidence. Real Confidence. Real Results.
Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
REAL WORLD EVIDENCE OVERVIEWReal World Evidence Quick Links
See markets more clearly. Opportunities more often.
Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
COMMERCIALIZATION OVERVIEWCommercialization Quick Links
Service driven. Tech-enabled. Integrated compliance.
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
COMPLIANCE OVERVIEWSafety & Regulatory Compliance Quick Links
Intelligence that transforms life sciences end-to-end.
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWTechnology Quick Links
CLINICAL PRODUCTS
COMMERCIAL PRODUCTS
COMPLIANCE, SAFETY, REG PRODUCTS
BLOGS, WHITE PAPERS & CASE STUDIES
Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSTHE IQVIA INSTITUTE
An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
SEE LATEST REPORTS
FEATURED INNOVATIONS
-
IQVIA Connected Intelligence™
-
IQVIA Healthcare-grade AI™
-
Human Data Science Cloud
-
IQVIA Innovation Hub
-
Decentralized Trials
-
Patient Experience powered by Apple
WHO WE ARE
- Our Story
- Our Impact
- Commitment to Public Health
- Code of Conduct
- Environmental Social Governance
- Privacy
- Executive Team
NEWS & RESOURCES
Unlock your potential to drive healthcare forward
By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
LEARN MORE
IQVIA AI is Healthcare-grade AI
Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.
LEARN MORE
Your healthcare data deserves more than just a cloud.
The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.
LEARN MORE
Innovations make an impact when bold ideas meet powerful partnerships
The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.
LEARN MORE
Proven, faster DCT solutions
IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
LEARN MORE
IQVIA Patient Experience Solutions powered by Apple
Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm. IQVIA and Apple are collaborating to bring this exciting future of personalized care directly to devices patients already have and use.
LEARN MOREWORKING AT IQVIA
Our mission is to accelerate innovation for a healthier world. Together, we can solve customer challenges and improve patient lives.
LEARN MORELIFE AT IQVIA
Careers, culture and everything in between. Find out what’s going on right here, right now.
LEARN MORE
WE’RE HIRING
"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.
SEARCH JOBSBlog
Testing Times for Health Technology Assessment (HTA)
Aug 31, 2020
With the ongoing coronavirus pandemic continuing to upend healthcare systems and economies around the world, health technology assessment (HTA) agencies have found themselves (unsurprisingly) in a difficult position. With healthcare priorities in many countries shifting towards the search for treatments that can help alleviate the effects of COVID-19, the disease caused by the coronavirus, many HTA organisations are facing difficult decisions on how best to allocate their scarce resources. Using IQVIA’s Pharma Pricing & Reimbursement service, this blog assesses the changing HTA landscape around the world.
Many HTA organisations face pressures on multiple fronts. Quite apart from the difficulties imposed by stringent ‘lockdown’ measures in many countries, designed to reduce the movement of citizens and so curb the virus’ spread, HTA agencies must deal with the fact that governments’ short-term healthcare priorities have changed. HTA bodies typically rely on the input of clinical experts when formulating their recommendations in relation to new medical technologies (including prescription drugs), but with health systems under unprecedented pressure, such experienced medical professionals are prioritising ‘front line’ medical care.
Thus, for example, the National Institute for Health and Care Excellence (NICE) in the UK (which produces guidance for healthcare providers in England, Wales and Northern Ireland) has advised that timelines for many of its ongoing drug appraisals are to be reviewed. Meanwhile, the Scottish Medicines Consortium (SMC) decided in spring to cancel all committee meetings that were to have taken place in the period April through June 2020 so that its members and staff could focus on front line care. The agency tentatively resumed technology appraisals in July 2020, but has continued to adopt a selective approach in terms of which technologies it prioritises for assessment, given the backlog that has built up. Similarly, the All Wales Medicines Strategy Group (AWMSG), which provides guidance on medicines not (yet) evaluated by NICE, decided to suspend its “normal business” through the end of May 2020 as a result of the pandemic.
Such disruption can be seen elsewhere, too. In Germany, the Institute for Quality and Efficiency in Health Care (Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen, IQWiG) has extended the comment and feedback periods for a number of ongoing assessments, although the agency is maintaining a full programme of evaluations. Denmark’s Medicines Council (Medicinrådet) has also warned of delays in its evaluations, though it is unable to predict when or where these may occur.
Not all HTA agencies are impacted in the same way, of course – reflecting not only the varying burden of COVID-19 in different countries, but also perhaps fundamental differences in the way in which HTAs are conducted, and the level of health system resource required. Ireland’s National Centre for Pharmacoeconomics (NCPE) and Portugal’s National Authority of Medicines and Health Products (Autoridade Nacional do Medicamento e Produtos de Saúde, INFARMED), for example, appear able to proceed with “business as usual” for now.
And despite the disruption, HTA bodies are turning their attention to providing advice to governments and health systems on tackling the virus itself. NICE has for example stated it is now prioritising the development of guidance in relation to the diagnosis and treatment of COVID-19 including the publication of new “rapid guidelines” developed expressly for this purpose. INFARMED and Poland’s Agency for Health Technology Assessment and the Tariff System (Agencja Oceny Technologii Medycznych i Taryfikacji, AOTMiT) have similarly produced a range of COVID-19 related guidance for healthcare providers.
HTA agencies in some countries could also be primed to take a more prominent role in public discussion of the virus. Indeed, in many ways HTA organisations are uniquely placed to deliver evidence-based information about how members of the general public should respond to the threat posed by COVID-19.
It has been widely observed that the speed of the virus’ spread around the world has been matched only by the deluge of misinformation that has accompanied it, a phenomenon that has been amplified by the ease with which such distortions can be shared via social media platforms such as Facebook and WhatsApp. It is significant, therefore, that the Canadian Agency for Drugs and Technologies in Health (CADTH) has devoted significant resources to developing a COVID-19 portal containing information only from “trusted sources” and aimed at a general audience, including advice on whether users should trust “Dr Google”. Evidence, perhaps, of how the coronavirus crisis may already be subtly shifting the HTA landscape.
IQVIA Pharma Pricing & Reimbursement (PPR) draws on decades of experience in the market access space to bring you the latest global developments in pricing and reimbursement. With access to IQVIA’s network of local offices, and extensive contacts within government and industry, the PPR service offers timely news and articles alongside comprehensive guides to P&R regulations around the world.