- OVERVIEW AND WHY SHOULD YOU ATTEND
- AREAS COVERED AND LEARNING OBJECTIVES
- WHO WILL BENEFIT
The European Medicines Agency plays a central role in the development and authorisation of medicines for rare diseases. These medicines are termed ‘orphan medicines’ in the medical world.
The EMA is responsible for reviewing applications from sponsors for the designation of medicines for rare diseases.
To benefit from the incentives, sponsors intending to develop an orphan medicine must submit an application to the EMA requesting 'orphan designation' for their medicine.
The application is evaluated by the EMA’s Committee for Orphan Medicinal Products (COMP), which provides its opinion on whether or not the medicine qualifies as an orphan medicine for the treatment, prevention or diagnosis of a rare disease. If the COMP issues a positive opinion, the European Commission may then grant the medicine orphan status.
Because rare diseases are a global issue, the EMA works closely with its international partners on the designation and assessment of orphan medicines.
The EMA works with organisations representing patients with rare diseases through the European Organisation for Rare Diseases (EURORDIS).
why should you attend
Orphan Drug lists are intended for the diagnosis, prevention or treatment of life-threatening or very serious conditions that affect no more than 5 in 10,000 people in the European Union.
Designation as an orphan medicinal product in the EU has important advantages. Sponsors who obtain orphan designation benefit from a number of incentives, including protocol assistance, a type of scientific advice specific for designated orphan medicines, fee waivers or reductions for the regulatory procedures or a 10 year market exclusivity once the medicine is on the market. Therefore, it is important for companies to know the process for designation.
In this Webinar the process for obtaining designation is explained in detail. There are many factors to consider when preparing an application, and taking those into account will ensure a smooth process. The main factors to consider are:
- Definition of a medical condition
- Dealing with subsets
- How to show significant benefit
Practical experience with the process (for instance about pre-submission meetings and the role of the Committee for Orphan Medicinal Products) is discussed and very valuable when preparing an application.
It is also important to be aware of the activities after orphan designation.
In addition, considerations for Marketing Authorisations of Orphan Medicinal Products will be discussed. The relevant guidelines and determinants for successful marketing authorisations of orphan medicinal products will be reviewed.Click to View the Pricing Plan
The Webinar will start with an introduction. It is estimated that today in the EU, 5-8000 distinct rare diseases affect 6-8% of the population - about 30 million people. Rare diseases are defined as life-threatening or chronically debilitating conditions that affect no more than 5 in 10,000 people in EU. This is equivalent to around 250,000 people or less for each disease.
These conditions occur so infrequently that the cost of developing and bringing to the market a medicinal product to diagnose, prevent or treat the condition would not be recovered by the expected sales of the medicinal product.
Patients suffering from rare conditions should be entitled to the same quality of treatment as other patients.
Since the pharmaceutical industry has little interest, under normal market conditions, in developing and marketing medicines intended for small numbers of patients it is necessary to stimulate the research, development and bringing to the market of appropriate medications by the pharmaceutical industry. Incentives for the development of orphan medicinal products have been available in the United States of America since 1983 and in Japan since 1993, and also the EU offers a range of incentives to encourage the development of these medicines.
In this webinar the legal background for orphan designation will be explained, as well as the composition and tasks of the COMP.
Guidance will be given regarding the criteria for designation, how to describe the medical condition, how to deal with subsets and how to explain the significant benefit of the product.
The procedure for obtaining designation as an orphan medicinal product will be described, as well as the timing of the designation.
The EMA maintains a searchable list of opinions on applications for rare diseases (orphan) designations.
Sponsors of designated orphan medicines are eligible to benefit from the incentives offered, including:
- Assistance with development of the medicine;
- Reduced fees for marketing-authorisation applications;
- Protection from market competition once the medicine is authorised.
Designated orphan medicines are assessed centrally on a European level by the EMA's Committee for Medicinal Products for Human Use (CHMP), rather than in each Member State separately. The guidelines for Marketing Authorisation procedures and determinants for successful Marketing Authorisations will be discussed.
- What an orphan medicinal product designation means
- What benefits the designation offers
- How to obtain designation
WHO WILL BENEFIT
- Regulatory Affairs Personnel
- Sponsor Senior management
- Project Managers
- Clinical Trial Heads
- Medical writers
- CRAs and CRCs
- QA / Compliance personnel
- Clinical Research Scientists
- QA / QC Auditors and Staff
Adriaan Fruijtier has graduated as a pharmacist at the University of Utrecht, The Netherlands. He is currently Director Regulatory Affairs at CATS Consultants. Until March 2004, he has been Head of the Oncology Group within Global Regulatory Affairs at Bayer AG, Wuppertal, Germany, and Bayer Corporation, West Haven, CT, USA. Between 2001 and 2003, he was Director of Regulatory Affairs at Micromet AG, a biotech company in Munich, Germany. Prior to joining Micromet he has worked for four years as a Project Manager for Oncology Projects at the European Medicines Agency in London, United Kingdom. He joined the European Medicines Agency from Novartis AG, Basel, Switzerland, where he was Regulatory Affairs Project Manager in the Oncology group in 1996 and 1997. Before 1996, he was Head of Drug Regulatory Affairs for six years at Ciba-Geigy in the Netherlands, and has worked as Manager Regulatory Affairs at Glaxo, also in the Netherlands.View all trainings by this speaker
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