Medical CPD Courses and Workshops Available
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Practical Solutions For Establishing In-Vitro In-Vivo Correlation
Pharmaceutical Training International (PTI)
IVIVC is a critical tool described in many guidelines and its usage in development is recommended to reduce the risk of in-vivo testing. This 2-day practical training course; led by... Read more
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Practical Solutions For Establishing In-Vitro In-Vivo Correlation Online Academy
Pharmaceutical Training International (PTI)
In-vitro in-vivo correlation is a critical tool described in many guidelines and its usage in development is recommended to reduce the risk of in-vivo testing. Led by Jean-Michel... Read more
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Project Management For Regulatory Affairs Professionals
Pharmaceutical Training International (PTI)
Recognized as a key criterion for success in many industries; effective project management may also be deployed to great effect within regulatory affairs. This course will provide you... Read more
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Regulatory Information Management & IDMP Training
Pharmaceutical Training International (PTI)
Over two days you will learn the key aspects of RIM and the new IDMP standard such as training and user compliance; outsourcing and data/content management. Once completed you will have... Read more
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Regulatory; Developmental And Manufacturing Challenges For ATMPs
Pharmaceutical Training International (PTI)
This two-day course will provide you with a practical understanding of regulatory challenges; manufacturing concerns and clinical trial preparation for ATMPs. Using case studies and... Read more
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Risk Based Monitoring And Targeted SDV Online Academy
Pharmaceutical Training International (PTI)
Implementing the most efficient strategies for monitoring is crucial to reduce the risks and costs associated with your clinical trial – it is estimated that sponsors can save 23%... Read more
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Understanding And Preparing The Quality And Pharmaceutical Module Of The Global Ctd Dossier
Pharmaceutical Training International (PTI)
This 3-day course will provide you with a clear understanding of the US and European regulatory requirements for Module 3 (CTD) of your application; and will show you how to compile... Read more
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