Time: 10:00 - 12:00 UK time Presenters: Jessica Purchase, Group Health Economics Manager (F. Hoffmann-La Roche Ltd, Welwyn) and Monica Daigl, HTA Statistician and Health Economist (F. Hoffmann-La Roche Ltd, Basel)
Abstract:
There is a simple equation for access in the UK: Access = Reimbursement + Uptake
Yet, whilst a simple and logical approach, each component is challenging to achieve.
This webinar focuses on the National Reimbursement side: the National Institute for Health and Care Excellence (NICE) - who they are, what is involved in the Health Technology Appraisal (HTA) assessment, how they make decisions.
We’ll also review where the devolved nations come in: how do the Scottish Medicines Consortium (SMC) and All Wales Medicines Strategy Group (AWMSG) differ from NICE in decision making?
Finally, through the use of a real world example, we’ll explore the key drivers and barriers experienced in decision making: specifically the challenges associated with correct comparators and predicting of long term outcomes.
This will lead to the second part of the webinar. We will focus on two advanced statistical techniques to inform health economic models: modelling of time to event endpoints such as progression free and overall survival beyond the duration of a clinical study to predict long-term outcomes; and network meta analyses to estimate the value of a drug in the absence of direct comparative evidence.
Finally, we provide our key recommendations for the future of clinical trial design, to support access for the UK market.
About the Presenters:
Jessica Purchase is a Group Health Economics Manager in the Health Economics and Strategic Pricing team in Roche UK. She joined Roche in 2016, following 5 years of Health Economics and Market Access consulting. In her role she has successfully lead on a variety of HTAs resulting in UK access in the oncology space.
Monica Daigl is a medical statistician and epidemiologist with >15 years of experience in the analysis of clinical trials and observational studies in pharma, medical device industry and academia. She joined 2014 the Global Access Center of Excellence at F. Hoffmann-La Roche as HTA Statistician and Health Economist. In her role she supports Roche affiliates with their local HTA submissions in multiple therapeutic areas.
Time: 10:00 - 12:00 UK time Presenters: Jessica Purchase, Group Health Economics Manager (F. Hoffmann-La Roche Ltd, Welwyn) and Monica Daigl, HTA Statistician and Health Economist (F. Hoffmann-La Roche Ltd, Basel)
Abstract:
There is a simple equation for access in the UK: Access = Reimbursement + Uptake
Yet, whilst a simple and logical approach, each component is challenging to achieve.
This webinar focuses on the National Reimbursement side: the National Institute for Health and Care Excellence (NICE) - who they are, what is involved in the Health Technology Appraisal (HTA) assessment, how they make decisions.
We’ll also review where the devolved nations come in: how do the Scottish Medicines Consortium (SMC) and All Wales Medicines Strategy Group (AWMSG) differ from NICE in decision making?
Finally, through the use of a real world example, we’ll explore the key drivers and barriers experienced in decision making: specifically the challenges associated with correct comparators and predicting of long term outcomes.
This will lead to the second part of the webinar. We will focus on two advanced statistical techniques to inform health economic models: modelling of time to event endpoints such as progression free and overall survival beyond the duration of a clinical study to predict long-term outcomes; and network meta analyses to estimate the value of a drug in the absence of direct comparative evidence.
Finally, we provide our key recommendations for the future of clinical trial design, to support access for the UK market.
About the Presenters:
Jessica Purchase is a Group Health Economics Manager in the Health Economics and Strategic Pricing team in Roche UK. She joined Roche in 2016, following 5 years of Health Economics and Market Access consulting. In her role she has successfully lead on a variety of HTAs resulting in UK access in the oncology space.
Monica Daigl is a medical statistician and epidemiologist with >15 years of experience in the analysis of clinical trials and observational studies in pharma, medical device industry and academia. She joined 2014 the Global Access Center of Excellence at F. Hoffmann-La Roche as HTA Statistician and Health Economist. In her role she supports Roche affiliates with their local HTA submissions in multiple therapeutic areas.
Time: 10:00 - 12:00 UK time Presenters: Jessica Purchase, Group Health Economics Manager (F. Hoffmann-La Roche Ltd, Welwyn) and Monica Daigl, HTA Statistician and Health Economist (F. Hoffmann-La Roche Ltd, Basel)
Abstract:
There is a simple equation for access in the UK: Access = Reimbursement + Uptake
Yet, whilst a simple and logical approach, each component is challenging to achieve.
This webinar focuses on the National Reimbursement side: the National Institute for Health and Care Excellence (NICE) - who they are, what is involved in the Health Technology Appraisal (HTA) assessment, how they make decisions.
We’ll also review where the devolved nations come in: how do the Scottish Medicines Consortium (SMC) and All Wales Medicines Strategy Group (AWMSG) differ from NICE in decision making?
Finally, through the use of a real world example, we’ll explore the key drivers and barriers experienced in decision making: specifically the challenges associated with correct comparators and predicting of long term outcomes.
This will lead to the second part of the webinar. We will focus on two advanced statistical techniques to inform health economic models: modelling of time to event endpoints such as progression free and overall survival beyond the duration of a clinical study to predict long-term outcomes; and network meta analyses to estimate the value of a drug in the absence of direct comparative evidence.
Finally, we provide our key recommendations for the future of clinical trial design, to support access for the UK market.
About the Presenters:
Jessica Purchase is a Group Health Economics Manager in the Health Economics and Strategic Pricing team in Roche UK. She joined Roche in 2016, following 5 years of Health Economics and Market Access consulting. In her role she has successfully lead on a variety of HTAs resulting in UK access in the oncology space.
Monica Daigl is a medical statistician and epidemiologist with >15 years of experience in the analysis of clinical trials and observational studies in pharma, medical device industry and academia. She joined 2014 the Global Access Center of Excellence at F. Hoffmann-La Roche as HTA Statistician and Health Economist. In her role she supports Roche affiliates with their local HTA submissions in multiple therapeutic areas.
Time: 10:00 - 12:00 UK time Presenters: Jessica Purchase, Group Health Economics Manager (F. Hoffmann-La Roche Ltd, Welwyn) and Monica Daigl, HTA Statistician and Health Economist (F. Hoffmann-La Roche Ltd, Basel)
Abstract:
There is a simple equation for access in the UK: Access = Reimbursement + Uptake
Yet, whilst a simple and logical approach, each component is challenging to achieve.
This webinar focuses on the National Reimbursement side: the National Institute for Health and Care Excellence (NICE) - who they are, what is involved in the Health Technology Appraisal (HTA) assessment, how they make decisions.
We’ll also review where the devolved nations come in: how do the Scottish Medicines Consortium (SMC) and All Wales Medicines Strategy Group (AWMSG) differ from NICE in decision making?
Finally, through the use of a real world example, we’ll explore the key drivers and barriers experienced in decision making: specifically the challenges associated with correct comparators and predicting of long term outcomes.
This will lead to the second part of the webinar. We will focus on two advanced statistical techniques to inform health economic models: modelling of time to event endpoints such as progression free and overall survival beyond the duration of a clinical study to predict long-term outcomes; and network meta analyses to estimate the value of a drug in the absence of direct comparative evidence.
Finally, we provide our key recommendations for the future of clinical trial design, to support access for the UK market.
About the Presenters:
Jessica Purchase is a Group Health Economics Manager in the Health Economics and Strategic Pricing team in Roche UK. She joined Roche in 2016, following 5 years of Health Economics and Market Access consulting. In her role she has successfully lead on a variety of HTAs resulting in UK access in the oncology space.
Monica Daigl is a medical statistician and epidemiologist with >15 years of experience in the analysis of clinical trials and observational studies in pharma, medical device industry and academia. She joined 2014 the Global Access Center of Excellence at F. Hoffmann-La Roche as HTA Statistician and Health Economist. In her role she supports Roche affiliates with their local HTA submissions in multiple therapeutic areas.
Time: 10:00 - 12:00 UK time Presenters: Jessica Purchase, Group Health Economics Manager (F. Hoffmann-La Roche Ltd, Welwyn) and Monica Daigl, HTA Statistician and Health Economist (F. Hoffmann-La Roche Ltd, Basel)
Abstract:
There is a simple equation for access in the UK: Access = Reimbursement + Uptake
Yet, whilst a simple and logical approach, each component is challenging to achieve.
This webinar focuses on the National Reimbursement side: the National Institute for Health and Care Excellence (NICE) - who they are, what is involved in the Health Technology Appraisal (HTA) assessment, how they make decisions.
We’ll also review where the devolved nations come in: how do the Scottish Medicines Consortium (SMC) and All Wales Medicines Strategy Group (AWMSG) differ from NICE in decision making?
Finally, through the use of a real world example, we’ll explore the key drivers and barriers experienced in decision making: specifically the challenges associated with correct comparators and predicting of long term outcomes.
This will lead to the second part of the webinar. We will focus on two advanced statistical techniques to inform health economic models: modelling of time to event endpoints such as progression free and overall survival beyond the duration of a clinical study to predict long-term outcomes; and network meta analyses to estimate the value of a drug in the absence of direct comparative evidence.
Finally, we provide our key recommendations for the future of clinical trial design, to support access for the UK market.
About the Presenters:
Jessica Purchase is a Group Health Economics Manager in the Health Economics and Strategic Pricing team in Roche UK. She joined Roche in 2016, following 5 years of Health Economics and Market Access consulting. In her role she has successfully lead on a variety of HTAs resulting in UK access in the oncology space.
Monica Daigl is a medical statistician and epidemiologist with >15 years of experience in the analysis of clinical trials and observational studies in pharma, medical device industry and academia. She joined 2014 the Global Access Center of Excellence at F. Hoffmann-La Roche as HTA Statistician and Health Economist. In her role she supports Roche affiliates with their local HTA submissions in multiple therapeutic areas.
Time: 10:00 - 12:00 UK time Presenters: Jessica Purchase, Group Health Economics Manager (F. Hoffmann-La Roche Ltd, Welwyn) and Monica Daigl, HTA Statistician and Health Economist (F. Hoffmann-La Roche Ltd, Basel)
Abstract:
There is a simple equation for access in the UK: Access = Reimbursement + Uptake
Yet, whilst a simple and logical approach, each component is challenging to achieve.
This webinar focuses on the National Reimbursement side: the National Institute for Health and Care Excellence (NICE) - who they are, what is involved in the Health Technology Appraisal (HTA) assessment, how they make decisions.
We’ll also review where the devolved nations come in: how do the Scottish Medicines Consortium (SMC) and All Wales Medicines Strategy Group (AWMSG) differ from NICE in decision making?
Finally, through the use of a real world example, we’ll explore the key drivers and barriers experienced in decision making: specifically the challenges associated with correct comparators and predicting of long term outcomes.
This will lead to the second part of the webinar. We will focus on two advanced statistical techniques to inform health economic models: modelling of time to event endpoints such as progression free and overall survival beyond the duration of a clinical study to predict long-term outcomes; and network meta analyses to estimate the value of a drug in the absence of direct comparative evidence.
Finally, we provide our key recommendations for the future of clinical trial design, to support access for the UK market.
About the Presenters:
Jessica Purchase is a Group Health Economics Manager in the Health Economics and Strategic Pricing team in Roche UK. She joined Roche in 2016, following 5 years of Health Economics and Market Access consulting. In her role she has successfully lead on a variety of HTAs resulting in UK access in the oncology space.
Monica Daigl is a medical statistician and epidemiologist with >15 years of experience in the analysis of clinical trials and observational studies in pharma, medical device industry and academia. She joined 2014 the Global Access Center of Excellence at F. Hoffmann-La Roche as HTA Statistician and Health Economist. In her role she supports Roche affiliates with their local HTA submissions in multiple therapeutic areas.
Registration:
Registration
PSI Member
Free
Non-member
£20 (plus VAT)
Registration has now closed.
Upcoming Events
Joint PSI/EFSPI Visualisation SIG 'Wonderful Wednesday' Webinars
Our monthly webinar explores examples of innovative data visualisations relevant to our day to day work. Each month a new dataset is provided from a clinical trial or other relevant example, and participants are invited to submit a graphic that communicates interesting and relevant characteristics of the data.
The event will open with an overview on drug development in women’s health from a clinician perspective. This talk is followed by talks about statistical challenges when planning IVF studies and analysing the menstrual cycles.
This webinar will provide an overview of surrogacy for licensing and reimbursement. In turn, the need of extensions of the SPIRIT and CONSORT statement will be defined and outlined, with case studies to support.
Joint PSI/EFSPI Pre-Clinical SIG Webinar: Virtual Control Groups in Toxicity Studies
Lea Vaas will present how replacement of concurrent control animals by Virtual Control Groups (VCGs) in systemic toxicity studies may help in contributing to the 3R's principle of animal experimentation: Reduce, Refine, Replace.
Joint PSI/EFSPI Data Science SIG Webinar: Developing Digital Measures (Digital Biomarkers) in Drug Development – insights from Mobilise D consortium
We will share a brief overview of what Mobilise D is and why it is an important step stone in the development of digital biomarkers, and how Mobilise D outputs can be relevant for you.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
PSI Webinar: Development of Gene Therapies: Strategic, Scientific, Regulatory and Access Considerations
This webinar will cover the history of cell/gene therapy, major regulatory advances, the role of quantitative scientists in drug development of these novel therapeutics, and discuss opportunities for innovation and product advancement.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
PSI Introduction to Industry Training (ITIT) Course - 2024/2025
An introductory course giving an overview of the pharmaceutical industry and the drug development process as a whole, aimed at those with 1-3 years' experience. It comprises of six 2-day sessions covering a range of topics including Research and Development, Toxicology, Data Management and the Role of a CRO, Clinical Trials, Reimbursement, and Marketing.
This networking event is aimed at statisticians that are new to the pharmaceutical industry who wish to meet colleagues from different companies and backgrounds.
Statisticians in the Pharmaceutical Industry Executive Office: c/o MCI UK Ltd | Unit 24/22 South | Building 4000 | Langstone Park| Langstone Road | Havant | PO9 1SA | UK