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Safe Aseptic Handling

This Safe Aseptic Handling training will help you to reduce the chance of contamination your cell culture or cell products.

Target group

  • Researchers who want to improve their cell/tissue culture skills.
  • Candidates who will have to start working in a downflow cabinet.

About Safe Aseptic Handling

Aseptic Handling means using practices and procedures to prevent contamination from pathogens. The core elements of aseptic handling are a sterile work area, good personal hygiene, sterile reagents and media, and sterile handling.

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Covered topics:

1

Classroom training: contamination sources & product impact

Incl. Personnel, Gowning, Environment, Equipment, Materials and processes
2

Hands-on Safe Aseptic Handling Techniques training in laminar flow cabinet

to be confirmed

3 hours

Medace facilities, Maastricht

1:1 Practical training

Lunch, coffee and drinks

Training Certificate

Experts

Dana Quaden – Quality Associate GMP at Medace

Dana Quaden is responsible for maintaining and improving the Medace’ Quality Management System according to the current cell therapy (GMP) legislation and regulations on a daily base. Dana provides guidance to the cell therapy clients with developing tailor-made quality documentation for the specific cell therapy processes, further development of manufacturing processes and trainings on general cleanroom activities.

Joppe Hermans – Biotech Associate at Medace

Joppe Hermans is responsible for providing advice, facilitation, and training to clients in GMP production. Besides this, he’s available to give hands-on support in GMP production and QC processes. This includes but is not limited to carrying out aseptic manufacturing procedures, writing and reviewing quality documentation, and validation of protocols.

Celeste Tillemans – Biosafety Officer / Operations & Logistics manager at Medace

Celeste Tillemans is the first point of contact for emerging companies working in the Medace facilities. Together with Chris Duxbury, Celeste manages the planning and all kinds of other operational matters. Her responsibilities also includes biological safety, for which Celeste is responsible as Biosafety Officer.

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About Medace

Medace supports academic groups and companies with innovative medical concepts in need of technical, quality and clinical expertise. Bringing along a broad network, we help you to successfully develop your product into the clinical phase. With our proven pick-and-choose concept we provide you clinical product development compliant with the latest ISO and GMP requirements.

Our specialists work together with you and your team in a fully equipped and state of the art biomedical co-working space – whenever it suits you. More about Medace.

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