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Showing 1 - 1 of 50 results
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Development phase
Basic Research
Basic Research
Early discovery
Early discovery
Non-clinical development
Non-clinical development
Clinical development
Clinical development
FDA/EMA review
FDA/EMA review
Post-market monitoring
Post-market monitoring
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Clinician
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/9
Data manager
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/6
Facility manager
15
/32
Patient representative
0
/6
Pharmacist
37
/64
QA personnel
21
/29
QC personnel
14
/21
Regulatory assurance expert
6
/20
Research nurse
0
/7
Scientist
38
/68
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30
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On Site
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/35
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Online
9
/47
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/62
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≤ 1 hour
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/17
1 - 4 hours
2
/13
1 day
7
4 - 8 hours
13
/17
Multi-day
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/30
Varies per course
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/6
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ATMP
7
/10
Business development
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CAR T
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/8
Cell technology
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/10
Cleanroom
7
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/14
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/11
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/19
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27
Paid
50
Free for members
9
Free, paid certificate
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PDA training courses
Multiple courses ranging from aseptic processing to biopharmaceuticals, cleaning, compounding, environmental monitoring, quality risk management system, lyophilization, parenteral packaging, etc
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GMP&GDP training courses
GMP and GDP
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GMP training courses
Aseptic production, microbiological quality control, quality assurance, pharmaceutical microbiology
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GMP courses
GMP, GDP, quality risk management system
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GMP training courses
Aseptic production, microbiological quality control, pharmaceutical microbiology
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Drug development
Drug development (main focus is small molecules)
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Immuno-oncology
Tumor immunology, check point blockades, CAR T and other novel therapies
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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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Summerschool Advanced In Vitro Models
Best practices of advanced in vitro models, regulatory aspects, (stem) cell biology and technologies for testing medicine and/or substance safety testing as well as how the results can be validated, translated and implemented into human medicine
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Summerschool 3D Printing and Biofabrication
Basics of 3D printing, biofabrication and an insight into the challenges encountered when translating 3D printing towards biomedical applications
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Introduction To ATMPs/CGT
Basics of cell and gene therapy, practical working with various cell culture equipments
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Lab techniques in cell biology
Cell culture, cell counting and analysis, biobanking, sterility tests, transfection, image analysis
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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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Pharmaceutical Development of ATMPs Training Course
Comprehensive overview of the regulatory, quality and good manufacturing practice (GMP) requirements to consider when developing advanced therapy medicinal products (ATMPs).
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Cell and Gene Therapy Bioprocessing
Challenges of translating scientific discoveries into medicinal products such scaling up lenti-viruses
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Advanced Therapies GMP Onboarding
Advanced course on GMP requirements, QMS, quality controls
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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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Multiples course about clean room monitoring and aseptic drug production
Aseptic production, microbiological quality control, pharmaceutical microbiology
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Summerschool Regenerative Medicine
Basics of regenerative medicine, stem cell biology and technologies as well as how this science is translated and implemented into patient care
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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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Market approval
Market approval
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Train-the-trainer in de Life Sciences
Training geven (on the job)
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Pharmaceutical Quality and Regulatory Affairs
manufacture, regulations and quality standards for the pharmaceutical and ATMP, GMP guidelines, Market access
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Intro tot kwaliteitszorg (QA) in de Life Sciences
Kwaliteitsmanagement in de life sciences
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Intro tot kwaliteitscontrole (QC) in de Life Sciences
Basisprincipes van Quality Control
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GDP voor de Responsible Person (RP) in de Life Sciences
Good Distribution Practices
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Leidinggeven vanuit kwaliteitsperspectief in de life sciences sector
Leidinggeven in GMP cultuur
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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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