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Advanced Cell Therapy Technology
Apply detailed theoretical cell therapy process knowledge to upstream, cell expansion, and downstream applications. Identify bottlenecks and troubleshoot your specific processes. Perform industry standard techniques related to cell therapy manufacturing, with an emphasis on T-cell processes. Implement strategies used for process optimization and evaluation.
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Advanced Therapies GMP Onboarding
Advanced course on GMP requirements, QMS, quality controls
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Advanced Therapy Manufacturing
Cell/gene therapy manufacturing, quality assurance, product development pathways, GMP compliance, Investigational Medicinal product dossier writing, biosafety
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Advances in Point-of-Care Manufacturing: Promise vs. Reality
regulatory landscape of cell and gene therapy products
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Aseptisch werken: de mindset die het verschil maakt
Basis microbiologie, de werking van een cleanroom, de verschillen tussen reinigen, desinfecteren, decontamineren en steriliseren, de verschillende soorten aseptische opstellingen (LAF, Biosafety, isolator, RABS), staalname en monitoring, persoonlijke hygiëne, aseptisch gedrag.
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ATMP manufacturing
This scientific webinar of the last ADVANCE Webinar series presents an overview of essential aspects of ATMP manufacturing.
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ATMP Manufacturing, From Process Development to the Patient
ATMP basic knowledge, auto vs. allo cell therapies, manufacturing steps, regulatory concepts closed vs open systems
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ATMP Market Access
This scientific webinar of the last ADVANCE Webinar series presents an overview of essential aspects of ATMP manufacturing - market access.
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Audit behaviour in de Life Sciences
Deelnemers krijgen praktische tools en do’s en dont’s aangereikt om effectief te communiceren met auditors.
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Basis Bioprocessing
Hoe worden levende cellen ingezet als productiemiddel voor het maken van een nieuwe generatie aan geneesmiddelen en gezondheidsproducten.
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Basis GMP
Fundamentele wetmatigheden van de farmaceutische industrie
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Basis GMP voor ATMP productie
Fundamentele wetmatigheden van een ATMP productie
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Basis in validatie
Uitleg over waarom regulatorische autoriteiten validatie verwachten
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Basis microbiologie, sterilisatie en cleanroom design
Kennismaking met microbiologie, bestrijdingstechnieken en cleanroomdesign
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Behandelen en schrijven van technische deviaties
Overzicht van hoe deviaties opgevolgd, onderzocht & gedocumenteerd kunnen worden
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Behandelopties voor DLBCL
Which patients are eligible for CAR T therapies focus on DLBCL
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Bioprocessing and Manufacturing of Gene and Cell Therapy Products Course
Basic knowedge about cell therapy, CART cells, dendritic cells (DC), mesenchymal stromal cells (MSCs), gene therapy, manufacturing and quality control, regulation and marketing, career coaching
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Biotechnology course
Quality control of monoclonal antibodies, registration process of biosimilars, immunogenicity
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CAR T Masterclass 2023
A refresher course for now and future CAR therpaies focused on hematological diseases
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CAR T-celbehandeling: ontwikkelingen en overwegingen
Overview of CART-therapies, eligiblity of CAR trials, what so you need to take into account for car trials
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CAR-T e-courses
different modules, ranging from patient selection, evaluation, treatments and follow-up, to collection of the starting material by apheresis, reception, delivery and administration
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CAR-T: Historical Perspectives, Manufacturing and Clinical Applications
CAR-T: Basics and application
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