Manufacturing training

...for the manufacturing of both sterile and non-sterile products. It looks at the legislation and guidance available, techniques employed to monitor pharmaceutical environments... Learn about: Testing techniques, Identification of non-conformity, Testing results interpretation...

...Please contact our team at to discuss an alternative pathway. This four day self-study course, Manufacturing in Microsoft Dynamics NAV 2013 provides students... Learn about: Microsoft Dynamics...

...management will be discussed. Course Overview The course provides an overview of the concept of validation as described in Annex 15 to Eudralex Volume... Learn about: Cleaning validation, Analytical method validation, Good Manufacturing Practice (GMP)...

...of Microsoft Dynamics AX 2012. Students will have the opportunity to use the application to perform typical end-user tasks. The intended audience is... Learn about: Production Logistics, Sales Training, Manufacturing Production...

...and the potential reputation and cost consequences of non-compliance. Starting with a brief consideration of the key elements of the proposed revisions to the... Learn about: Management Operations, Quality Training, Regulatory Compliance...

...and partners that want to learn more advanced features and functions offered in Microsoft Dynamics AX 2012 Trade and Distribution feature areas... Learn about: Sales Training, Microsoft Dynamics...

...Numerous practical exercises are run throughout, providing clear demonstrations of techniques to employ - and pitfalls to avoid! Course Overview This practical... Learn about: Sampling and testing techniques, Analytical method validation, Pharmaceutical manufacturing...

...QPs face in industry today. Course Overview Our QP Roadshows explore what is involved in becoming a Qualified Person (QP), discussing the level of commitment... Learn about: Assessment process, Pharmaceutical Industry, Good Manufacturing Practice (GMP)...

...system and is an essential GMP requirement. It is critical that anyone dealing with GMP documents and documentation systems understand the regulatory requirements... Learn about: Best Practice for Documentation, Quality Management Systems, GMP Documentation...

...the challenges and risks involved in packaging operations in the Pharmaceutical Industry. A significant percentage of all product related complaints... Learn about: Pharmaceutical manufacturing, Qualified Person (QP), Packaging materials...

...an extensive introduction to the regulatory requirements governing pharmaceutical clean room operation, and details the aseptic filling and terminal sterilisation... Learn about: Clean room design, Quality Testing, Sterile Products Manufacture...

...based principles and regulatory guidances in the EU and US. Course Overview Successful completion of this one day course provides the delegate with understanding... Learn about: Pharmaceutical manufacturing, Quality Risk Management (QRM), Regulatory Guidelines...

...and delegates are supported by regular constructive feedback. This 5 day residential course is focused on providing you with the knowledge and skills required to perform first... Learn about: Internal/External Audits, ISO 9001, Quality Management Systems...

...Suitability The course is suitable for people who are responsible for preparing external inspections and those requiring knowledge and understanding of the inspection process... Learn about: Inspection Observations, Regulatory Compliance, Quality Process...

...legislation and guidelines for control of manufacture of medicines in the EU. This will help you ensure that all requirements are implemented in a practical... Learn about: Data Integrity, Industry insights, GMP update...

...interactive and also features several real-life case studies. Course Overview This stimulating course systematically builds up the knowledge of delegates... Learn about: Goods exportation, Quality Training, Goods importation...

...GDP, ISO 9001) are described briefly but not explored in depth. Course Overview This course provides an introduction to the requirements of internal auditing... Learn about: ISO 9001, Quality auditing, Good Manufacturing Practice (GMP)...

...pharmaceutical ingredients (APIs). The course is focused on the requirements of ICH Q7 and EU GMP Part II and the expectations of regulatory bodies both in the USA and Europe... Learn about: Problem Solving, Regulatory Compliance, Communication Skills...

...It will be of benefit to those working in sterile products manufacturing, QC (especially enviromental monitoring personnel) QA personnel as well as support engineers...

...This stimulating course systematically builds up the knowledge of delegates over three intensive days. It covers the regulations and guidelines associated...