Barrier Systems - This conference is part of Pharma Congress 2020

Barrier Systems - This conference is part of Pharma Congress 2020

Neuss, Germany

Course No 17896



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This is why you will benefit from attending this conference:
- Case studies from various pharmaceutical companies will deal with
- the implementation, qualification and operation of Isolator and RABS systems.
- You will discuss the current state of the art and new technological developments in Barrier Systems technology.
- You will get to know first hand the new EU-GMP Annex 1 draft requirements on Barrier Systems
- Experts from pharmaceutical companies will share their knowledge regarding operational experience.


The protection against microbial contamination is the most important point for drugs produced by aseptic processes. Today the regulators require a more strict separation between operators and product in the form of an access barrier.

Two systems are on the market – RABS (Restricted Access Barrier System) and Isolators. But only isolators are referred to by the US FDA as advanced aseptic Technology.
This conference will focus on current questions of barrier systems coming from FDA regulations as well as from the revised EU-GMP Annex 1, and it will specifically address the subject from the perspectives of pharmaceutical operators, planners and engineers.

Target Group

This event is directed at decision-makers from pharmaceutical production, development and quality assurance/control. It also addresses
engineers and planners who need to be well informed about current developments in the field of barrier Systems.


Congress Keynote: Case Study AbbVie: The new Biologics Site in Singapore
Dr Rolf Ratke | Ronan McGarvey, AbbVie
Grey Field Project for Production of Large Scale Bacterial antigen in an Aseptic Environment
Udara Yapa, MSD Animal Health Danube Biotech
- Planning, execution, commissioning and qualification and the technologies behind the vision
- Details of the Bacterial Antigen Production Line
- Challenges/complications and the complexity of the project
- Aseptic technology related to isolators will be discussed along with the single use connectors used in the process to maintain the containment of the Project

Aseptic processing and filling of a viral vector for gene and cell therapy
Leslie Southam, Oxford Biomedica
- An integrated solution of a state of the art small batch filler in a barrier system, designed to fit a biological production process: Freeze/thaw and time restrictions of the product lead to a Special line layout where formulation and filling are combined in one barrier system
- Application of No-touch-transfer (NTT): An alternative methodology to introduce pre-sterilized product containers into the Grade A environment without in process disinfection steps
- Aseptic Containment Approach: Requirements on containment driven by cross contamination control are combined with requirements for aseptic filling and viral Containment

Barrier Systems and Annex 1:  GMP inspectors’s point of view
Dr Daniel Müller, Local GMP Authority of Baden-Württemberg
- Most important changes of Annex 1 – an update
- Regulatory comparison of Annex 1 version 2018 and new / intended Annex 1
- GMP inspector’s comments on new / intended requirements for barriers

New-Designed Isolator for Aseptic Filling
Quentin Majeau, Hydro-Fill
- Isolators : Overview
- Disposable Isolator to a Virtual-wall Isolator
-Virtual wall Isolator : containment or Class A operation
-Virtual wall Isolator : Integration on a disposable filling line

Vaccines for the World - Insights into Design and Execution of a BSL2 Fill-Finish Facility
Rutger Vandiest, Bavarian Nordic
- The fill & finish operations for viral vaccines: specific attributes to facility and equipment
- Design, construction and qualification of their new fill & finish facility in Denmark
- Filling and lyophilization of live vaccines in a BSL2 environment
- Dedicated capacity for CDMO Services

Writing User Requirement Specifications (URS) for Isolator projects
Dr. Timo Krebsbach, HHAC Labor Dr. Heusler
- The URS should define clearly and precisely, what the user wants the equipment to do in terms of performance characteristics, product quality metrics, and production yields. It should also define any nonfunctional requirements,
constraints, and deliverables that need to be supplied with the system.
- The presentation shows the lesson learned from the view of a customer. 
- In the future topics like automation and digitalization need more attention from the very beginning

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