"Cleanroom technology in the manufacturing environment of medical devices"

Due to the new requirements imposed by ISO 13485 for the manufacturing and quality management of medical devices, cleanroom technology is becoming increasingly important. But how much cleanroom technology is really sensible, and how can it be implemented efficiently?

This central question cannot be answered easily due to the differentiated requirements for each product. The basis is solid knowledge about the relationships between airflow and sources of contamination, as well as the production process and operators, and the resulting material and personnel flows. We invite you to engage intensively with this topic in our new branch in Frickenhausen, both in theory and practice.

The Program:

Integrated Cleanroom Technology
Flexible - Future-proof - Sustainable

New Regulatory Requirements for Medical Devices
ISO 13485 and the new MDR - regarding the requirements for cleanrooms

Lunch Break

Efficient Climate Technology in the Cleanroom Environment

Roadshow on Filter Energy Efficiency
New ISO 16890
Handling of Filters

Excursion "Cleanroom Technology"
- Industry 4.0 in Cleanroom Planning
Risk Analysis with Virtual Reality Technology

- Practical Measurement Technology
- Handling of LF Devices
- Workshop: Gel Filter Replacement

The Essentials at a Glance:

Thursday, November 22, 2018, from 9:00 AM

Venue:
bc-technology GmbH
Carl-Zeiss-Straße 4
72636 Frickenhausen

Registration with:
Ms. Silke Ernst
s.ernst(at)bc-technology(dot)de
+49 7022 / 279 71-167

Participation is free of charge