Exhaust gas purification with cryocondensation
The Hof CryoProphase is the most future-proof, fail-safe and efficient solution for waste gas treatment in pharmaceutical and industrial processes. The user-friendly cold air technology enables a flexible condensation temperature as well as fast commissioning and low service costs.the CryoProPhase has a modular design, which allows a flexible design of the process and makes optimum use of installation space.for example, the process lines can be placed decentrally, [...].
Acceptance criteria for the purity of medical devices
- Regulatory and normative requirements for the cleanliness of medical devices - Current handling of cleanliness requirements by medical device manufacturers - New approaches to deriving acceptance criteria for the particulate and chemical cleanliness of medical devices - Next steps on the way to establishing an accepted approach.
HOF Sirius: Robot-based loading and unloading system
The requirements in the area of automatic loading and unloading of a freeze dryer are growing rapidly. Pharmaceutical products and primary packaging materials must be transported safely, optimally and in an integrated manner. Based on these requirements, HOF, as the specialist market leader, will present a newly developed innovative robot-assisted loading and unloading system at ACHEMA 2022. The HOF SIRIUS impresses with its innovative technological character and [...]
Risk minimization in cold WFI production
This presentation is about cold WFI production, the risks and how these can be reduced with the help of sanitization measures.
Climate conditioning of highly toxic APIs
Biopharmaceuticals offer numerous innovative possibilities for combating complex diseases. A key function is the ability of the active ingredients to influence the immune system in a targeted manner. These biotechnologically produced and modified active ingredients are highly potent and require safe protection of personnel during production. The manufacturing process for these products is very complex, as the active ingredients are usually produced under constant and sometimes [...]
Furnishing cleanrooms correctly: Choice of materials and design
The installation of personnel airlocks and cleanrooms offers a wide range of possibilities while at the same time numerous guidelines and specifications must be observed. The presentation will examine the special requirements placed on the furnishing of cleanrooms and personnel airlocks by both authorities and users and how these can be met. It will be shown which materials are usually [...]
DryClean-CAPE® - Flexible, lightweight dry cleaning room
Together with Cellforce Group, a research team from Fraunhofer IPA has developed a mobile dry cleaning tent. The so-called DryClean-CAPE® not only creates a clean production environment, but also one with low humidity. This factor plays a decisive role in product quality, particularly in battery cell and automotive production, but also in the aerospace industry. Together with Cellforce Group [...]
Hygienic Design: Bactus and his buddies
Introduction to the basic principles of hygienic design using a case study from Food and Pharma and Bactus and its buddies.
Primary validation of an RMM
The key to using an RMM (Rapid Microbiological Method) to monitor pharmaceutical water production is validation. The AQU@Sense MB is the first commercially available device that has successfully undergone primary validation. This presentation summarizes the methods and results of the validation.
Risk analysis
What does a risk analysis for an aseptic packaging line look like? What is expected by the health authority, how do you meet the requirements? Which standards are considered and are relevant in a risk analysis for aseptic filling machinesWho should be in the team? When is the best time for a risk analysis and how long does it take? What does such a document [...]