BioPharma training I Medical Device training I BioPharma Maintenance

ISO 13485 : 2016

20 Jun 2017

NSF Propose a training program including ISO 13485 : 2016 and MDSAP requirements ...

Stérilisation autoclave - principes de stérilisation

20 Jun 2017

Sélection de formations sur les autoclaves, les différents principes de stérilisations et les applications.

Vibration analysis ISO 18436-2

20 Jun 2017

Discover training program from I-Care - Maintenance specialist - in the field of vibration analysis

Active Pharmaceutical Ingredients - QP Module

12 Jun 2017

This course gives a unique insight into the regulatory expectations associated with producing both chemically synthesized APIs and biological/biotech APIs.

Pharmaceutical compressed air - Quality GMP standards and requirements

11 Jun 2017

This webinar will take you through the primary sources of compressed air contamination. It will also detail GMP standards and requirements pertaining to compressed air quality.

Validation and use of cloud Computing in FDA Regulated Environments

11 Jun 2017

This webinar will discuss FDA requirements related to cloud computing. It will provide step-by-step recommendations for using 'clouds' from planning to reporting.

Computer system validation - Reduce Costs and Avoid 483s

11 Jun 2017

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.