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: Identification of non-conformity, Pharmaceutical manufacturing, Testing techniques...

...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: Regulatory Compliance, Cleaning validation, Analytical method validation...

...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: Sales Training, Production Logistics, Microsoft Dynamics...

...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: Pharmaceutical manufacturing, Auditing documentation, Good Manufacturing Practice (GMP)...

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

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

...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: Pharmaceutical Industry, Requirements and expectations for QP Sponsors, Training Programme...

...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, GMP Documentation, Archiving and retrieval...

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

...an extensive introduction to the regulatory requirements governing pharmaceutical clean room operation, and details the aseptic filling and terminal sterilisation... Learn about: Sterile Products Manufacture, Aseptic filling and terminal sterilisation methods, Contamination risks...

...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: Quality Risk Management (QRM), Pharmaceutical manufacturing, Quality Training...

...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: ISO 9001, Pharmaceutical manufacturing, Internal/External Audits...

...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: Pharmaceutical manufacturing, Inspection Observations, Inspection 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: Regulatory Compliance, Legislation and guidelines update, Quality Training...

...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 Systems, Quality Training...

...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: External auditing, Confidence Training, ISO 19011...

...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: Communication Skills, Auditing documentation, Report Writing...

...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...