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  • Using the Human Protein Atlas – Tips and Tricks

    3 December 2016

    San Francisco, United States of America

    Using the Human Protein Atlas – Tips and Tricks https://tess.elixir-europe.org/events/using-the-human-protein-atlas-tips-and-tricks Organizer: Tove Alm, KTH Royal Institute of Technology This practical workshop will give you knowledge on why and how to use the Human Protein Atlas database (www.proteinatlas.org). The Human Protein Atlas portal is a publicly available database with millions of high-resolution images showing the spatial distribution of proteins in normal human tissues, cancer tissues, and different human cell lines. Antibody-based methods have been used together with transcriptomic analysis to explore the human proteome. The data are publicly available and include application-specific validations for each antibody. During the workshop different areas of the Protein Atlas will be explored, with a focus on the new Cell Atlas launching Dec. 4, 2016. Practical questions will be handed out that are solved by hands-on use of the Human Protein Atlas. Presentations: 1:30-1:35 pm – Welcome. Tove Alm, KTH Royal Institute of Technology 1:35-1:55 pm – Introduction to the Human Protein Atlas. Mathias Uhlén, KTH Royal Institute of Technology 1:55-2:15 pm – Spatial localization of proteins in the Tissue Atlas. Cecilia Lindskog, Uppsala University 2:15-2:35 pm – All about the Pathology Atlas. Fredrik Pontén, Uppsala University 2:35-2:45 pm – Break 2:45-3:05 pm – High-resolution: The Cell Atlas. Emma Lundberg, KTH Royal Institute of Technology 3:05-3:25 pm – Antibody validation for bioimaging. Lars Björk, KTH Royal Institute of Technology 3:25-3:45 pm – Working with the downloadable Human Protein Atlas data. Kalle von Feilitzen, KTH Royal Institute of Technology 3:45-3:55 pm – Concluding remarks and future prespective. Mathias Uhlén, KTH Royal Institute of Technology 3:55-4:10 pm – Break 4:10-5:30 pm – Practical session with General Questions and Answers 2016-12-03 13:30:00 UTC 2016-12-03 17:30:00 UTC ASCB 2016 Moscone Center, San Francisco, United States of America Moscone Center San Francisco San Francisco County United States of America Protein databases Protein expression [] Tove Alm, KTH Royal Institute of Technology tove.alm@scilifelab.se [] Life Science Researchers meetings_and_conferencesworkshops_and_courses [] protein family databasesImaging
  • Filing Variations in the European Union

    18 - 19 October 2017

    Berlin, Germany

    Filing Variations in the European Union https://tess.elixir-europe.org/events/filing-variations-in-the-european-union The course is designed to provide individuals with an in-depth awareness of the rules and procedures for filing variations and extensions. Understanding and applying the rules will ensure that you can file the variations successfully and avoid rejections. The course will also provide the attendee with a thorough knowledge of the following topics: •Overview of the different types of variations and the different procedures for a Marketing Authorizations in the EU •The different types of variations (Type IA, Type IB, Type II) •Variations involving product information •How to deal with unclassified variations •Line extensions •Work-sharing 2017-10-18 09:00:00 UTC 2017-10-19 17:00:00 UTC The Center for Professional Innovation & Education The Berlin Hilton, Berlin, Germany The Berlin Hilton Berlin Germany [] info@cfpie.com The Center for Professional Innovation & Education PharmaceuticalMedical DeviceBiotech 20 workshops_and_courses [] filing variations and extensionsMarketing Authorizations types of variationsunclassified variationsLine extensions
  • Medical Device Validation Training for Professionals

    18 - 20 October 2017

    Berlin, Germany

    Medical Device Validation Training for Professionals https://tess.elixir-europe.org/events/medical-device-validation-training-for-professionals Participants will learn how an effective Process Validation system is a critical requirement to the movement toward a risk-based approach to compliance and product safety. Also to be discussed is how to tackle process validation for medical device combination products. Issues to be covered include: •Learn how poor validation procedures and practices can lead to regulatory actions from regulators •Assurance of product quality derived from a compliant validation program •Learn how to improve process system knowledge and understanding •Learn methods for developing process validations and best practices •Understand the scope of regulations governing process validation and identify gaps •Develop a plan to rectify existing validation plans, protocols and reports •Learn how to implement and deploy a master validation plan 2017-10-18 09:00:00 UTC 2017-10-20 15:00:00 UTC The Center for Professional Innovation & Education The Berlin Hilton, Berlin, Germany The Berlin Hilton Berlin Germany [] info@cfpie.com The Center for Professional Innovation & Education Medical DeviceRegulatory AffairsQuality Assurance & ControlCompliance Engineering 20 workshops_and_courses [] Process ValidationRiskvalidation planscombination productsMedical Device
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