Kursussøgning, efter- og videreuddannelse – Københavns Universitet

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Kursussøgning, efter- og videreuddannelse

Market Access for Pharmaceutical Products – trends and challenges

Practical information
Study year 2016/2017
Time
Summer
Price

DKK 19,000/EUR 2,600. Fee includes teaching, course materials, all meals during course and examination.

Programme level Part Time Master
ECTS 3 ECTS
Course responsibles
  • Lourdes Cantarero Arevalo (13-797c823b706e7b816e7f727f7c4d80827b713b78823b7178)
  • Janine Marie Traulsen (15-6c63706b706730767463776e7567704275777066306d7730666d)
Course co-director: Marlene Gyldmark, Head of Modelling, Outcomes Research, Statistics and Epidemiology, F. Hoffmann-La Roche AG
  • Department of Pharmacy
Course number: SMIMIF115U

Course content

This course will provide insight into the key principles and a practical understanding of ‘market access’ as it relates to the pharmaceutical industry. The course starts with an overview of the key stakeholders and current trends in the global market access of pharmaceuticals followed by a review of the hot topics, challenges and relevant issues through a combination of lectures, discussions, group work, and case studies.

The topics include:

  • Introduction to market access - Marketing trends, defining global market access for the 21st century, its importance for optimizing product launches & its implications for the entire organization
  • Core concepts of market access – defining the concepts, theories and methods relevant for the pharmaceutical industry
  • Value generation – the role of clinical trials, real-world evidence, life-cycle management, health economics
  • Stakeholders – who they are, what are their perspectives, how and when to engage with “payers”
  • Health economic aspects of marketing – economic and financial considerations, core concepts and vocabulary
  • Pricing and reimbursement – global vs. local optimization, reference pricing systems in various markets.
  • Competencies – which skills and training are necessary to develop effective personnel; cross-functional teams
  • Patient centricity – the importance of understanding that the end-user must be the focal point during the entire process

Learning outcome

On completion of the course participants should be able to:

Knowledge

  • Explain how health policy affects and creates a framework for market access and the use of pharmaceuticals
  • Identify and describe the key challenges of obtaining market access
  • Identify major stakeholders & their influence on the drug reimbursement and prescription process.
  • Explain, reflect upon, and discuss the importance of market access and its relation to the entire pharmaceutical organization

 

Skill

  • Evaluate the relationship and dynamics of regulatory policies, and their implications for reimbursement of new pharmaceutical products
  • Describe, assess and discuss the various perspectives and potential conflicts of major actors associated with pharmaceutical market access

 

Competence

  • Participate in professional multi-disciplinary groups and be able to contribute with a market access perspective on pharmaceuticals

Recommended prerequisites

The course is for professionals working in the field of pharmaceuticals. It is intended as continuing professional development for professionals in the pharmaceutical industry, particularly in regulatory affairs, medical affairs and sales and marketing, including decision-makers and administrators in the public and private sectors. The course offers an excellent introduction for those less familiar with market access and will provide a deeper understanding for those with experience within administration and marketing. Please note, however, that the course is not an advanced course for market access specialists.

Mandatory prerequisites

Applicants must meet the following criteria:
• A relevant bachelor degree or equivalent
• A minimum of 2 years of relevant job experience
• Proficiency in English

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Apply here
 

Education

Master's Programme in Industrial Drug Development - elective

The course is preapproved as an elective in the Master of Industrial Drug Development (MIND) programme, the Master of Pharmaceutical Regulatory Affairs (MPRA) programme and Master of Drug Management (MDM) programme and open for freelance students who meet the admission criteria.

In the competitive world of pharmaceutical sales, developing a market access strategy and communicating the value of the brands to the ‘payers’ is at the top of the agenda. In recent years, the field of pricing and reimbursement of pharmaceuticals has become more complex and challenging.
The economic crisis, austerity measures and general demographic changes (aging population) coupled with newer and more expensive drugs has contributed to bigger hurdles in securing market access. Decisions are now increasingly made on cost-effectiveness and cost-containment rationales, whereas only safety and efficacy guided the decision to a greater degree years ago.

Although everyone seems to be talking about market access, very few are able to define it. Who are the new key stakeholders, exactly? Is it no longer the prescribers that decide which drug a patient should use? Is market access only about containing costs for the public budgets or are the benefits for patients and society as well?

Studyboard

Study Board for Part-time Master’s Programmes of Pharmaceutical Sciences

Course type

Part time Master and Diploma courses

Teacher

Torsten E. Christensen, Director, Market Access – Value Communication Novo Nordisk A/S
Jørgen Clausen, Chief Economist, The Danish Association of the Pharmaceutical Industry
Ulla Kirkegaard Madsen, Pharmacist, Executive Secretariat, Pharmacies and Reimbursement Division, Danish Health and Medicines Authority
Finn Børlum Kristensen, Secretariat Director, EUnetHTA Secretariat
Signe Høngaard Thybo, Healthcare Partnering Manager, Roche a/s Denmark
Elvira Mueller, Vice President Market Access and Health Economics, LA-SER Group, Germany

Additional speakers may be included.

Duration

22-26 August 2016

Schedulegroup

5 days
---- SKEMA LINK ----

Teaching and learning methods

The course is organized as an intensive 10-day course and comprises lectures, group discussions, presentations and discussions. In order to emphasize the flow of the process, the course is to a large extent based on the use of cases in both lectures and assignments.

Capacity

25 participants

Language

English

Literature

The compulsory syllabus comprises a collection of review papers, textbook chapters and case studies corresponding to approximately 500 pages (extra 200 pages self-selected literature for the optional term paper).

Workload

Category Hours
Preparation 22,5
Class Instruction 40
Exam 20
English 82,5

Exam (SMIMIF015E)

Type of assessment

Written assignment
An essay (case study) based on an extended literature list. The essay must be 8-15 pages.

Marking scale

passed/not passed

Criteria for exam assessment

To pass the exam the students should demonstrate the following:

Knowledge

  • Explain how health policy affects and creates a framework for market access and the use of pharmaceuticals.
  • Identify and describe the key challenges of obtaining market access.
  • Identify major stakeholders & their influence on the drug reimbursement and prescription process.
  • Explain, reflect upon, and discuss the importance of market access and its relation to the entire pharmaceutical organization.

 

Skill

  • Evaluate the relationship and dynamics of regulatory policies, and their implications for reimbursement of new pharmaceutical products.
  • Describe, assess and discuss the various perspectives and potential conflicts of major actors associated with pharmaceutical market access.

 

Competence

  • As a professional, be able to participate in multi-disciplinary groups and be able to contribute with a market access perspective on pharmaceuticals

Censorship form

No external censorship

Exam period

Deadline for submission of essay: 30 September 2016 at 16:00

Re-exam

Announced at the MIND programme's webpage.

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