Hotel Bildungszentrum 21 , Basel, Switzerland
May 21 2012 8:00AM - May 23 2012 3:30PM
This 3-day training course focuses on the highly important contribution of biopharmaceuticals to new drug development. As the functions of biopharmaceuticals are fully explored and utilised, they will become increasingly relevant to the drug development community.
Serious estimates suggest that 30% to 50% of newly authorised medicinal products are biopharmaceutical in nature. Biopharmaceuticals stem from a biological source with their protein structure transcribed from genetic information and expressed by a living cell. They are usually large and complex and their quality is determined by the manufacturing process where consistency and stability are extremely important. Biopharmaceuticals are pleiotropic and immunogenic and their non-clinical pharmacodynamic and safety characterisation is often hampered by lack of relevant animal models. Advanced Therapy Medicinal Products (ATMPs) are examples of innovative technologies used to develop and manufacture biopharmaceuticals. All these factors have implications for the way biopharmaceuticals are developed and regulated. European pharmaceutical legislation contains regulations specific to biopharmaceuticals and these will be covered in this course.
The course introduction provides an overview of both classical and biotechnology derived medicinal products and on the pathways used for scientific advice, clinical trials and marketing authorisations in Europe. The course will also cover in detail the particular requirements for the CMC section, comparability packages, and the important safety procedures required for infectious agents.
The particular aspects of the non-clinical and clinical development of biopharmaceuticals will be presented. A case study discussing how to develop a protein, without the relevant animal model, will also be examined. Case studies on monoclonal antibodies will illustrate the approach taken to identify benefit/risk ratio. An overview will be given on the most essential issues relating to ATMPs. A detailed presentation of the specific considerations for the development of biosimilar medicinal products, part of the EU provisions related to biopharmaceuticals, will be given during the course.
Key Topics - Definition and characteristics of biopharmaceuticals
- Topics of particular relevance to biopharmaceuticals such as comparability, immunogenicity, adventitious safety, bioassay
- ATMPs
- Biosimilar medicinal products
- Modules 3, 4 and 5 of the EU CTD of biopharmaceuticals
- Regulatory pathways for scientific advice, clinical trials and marketing authorisations of biopharmaceuticals
Learning Objectives:
At the conclusion of this training course, participants should be able to: - Identify the relevant stakeholders and pathways for regulatory submissions in the EU
- Describe the unique approach required to develop and to authorise complex biopharmaceuticals, compared to conventional pharmaceutical products
- Describe the key quality issues specific to biopharmaceuticals and apply them to the regulatory process
- Identify the implications of changes in the manufacturing process on the quality of the product
- Identify the relevant documentation for the non-clinical and clinical parts of submissions of biopharmaceuticals
- Explain the particulars of, and the data requirements specific to, the main product classes of biopharmaceuticals, ATMPs and biosimilars
- Understand common flaws in regulatory submissions and best practices relevant for European submissions
Target Audience:
Regulatory affairs and clinical research professionals who wish to focus their career on biopharmaceuticals or who wish to update their existing knowledge. This course is particularly relevant to junior and intermediate level regulatory affairs professionals.
Event Code:
12559
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