This one-day Validation training workshop is designed to provide an overview of the current concepts and guidance documents for Validation as defined by the US FDA in 2011 and PIC/S...
PharmOut has been training on Computer Systems Validation since 2008, much has changed recently, surprisingly Data Integrity remains a hot topic with regulators. This course examines the latest GAMP 5...
This CAPA Workshop is designed to provide you with an overview of a typical Corrective Action and Preventive Action (CAPA) program to handle outputs as part of a Pharmaceutical Quality...
We are offering a 1-day training course covering the essential “what you need to know” when it comes to GMP Part I Manufacturing Medicinal Products. Learn about the key requirements...
This one-day ISO 13485 workshop covers the requirements of ISO 13485 and its implications within a medical device manufacturing company. PharmOut’s consultants regularly design and write Quality Management Systems for...
This Good Distribution Practice (GDP) Training is designed to cover the latest GDP requirements in the distribution and/or warehousing of Active Pharmaceutical Ingredients (API) and medicinal products. It covers the...
This introductory one-day workshop will cover the key concepts of ISO 14971 and how to apply the standard to the medical devices industry.
Well written technical SOPs help employees understand information the first time they read or hear it. Who doesn’t want to improve compliance, shorten induction time and reduce deviations caused by...
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