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 Quality Risk Management (QRM) course is focused on how the QRM regulations apply to everyday pharmaceutical and biotech manufacturing processes and to accurately assess the risk to product quality...
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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Phone: +61 3 9887 6412
Email: info@pharmout.net
