This conference is designed to meet the wants and needs of the professionals from the pharmaceutical, generics and biotech companies involved in all aspects of regulatory affairs in Europe including:
• Regulatory Affairs
• Quality Assurance
• Quality Control
• Research and Development
• Product information
• Pharmaceutical Development
• Drug Registration
• Medical Development
• Pharmaceutical Registration
• Pharmaceutical Licensing
• Marketing Authorisations
• Clinical Trials
• Clinical research
• Drug Safety
As well as…
• PA’s to Regulatory Affairs Managers
• Support Staff
PROLOCAINE: A Stimulated Case Study
Prolocaine is a stimulated new blockbuster designed to be used for pain relief. Follow the stages of this drug through practical break out sessions to help you learn about the discovery, development and marketing process
"The speakers were very knowledgeable and interesting"
"Fantastic overview of all important aspects of the pharmaceutical industry"
"Worth the time off the field, allowing a rapid understanding of the global pharmaceutical industry particularities"
"High level speakers (mention to Charle Christy, Peter Warne, Katie Mc Connel, Anil K Dhiri)"
"A truly interesting mix of applicable topics and areas within the European pharmaceutical industry"
"A very useful overview of the industry, some great presenters with useful information. Excellent use of a valuable three days worth of time. I would recommend it to colleagues"
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Connect with the PTI faculty! PTI is a global pharmaceutical training company with over 60 interctive courses focusing on Regulatory Affairs, R&D, Clinical, Business Strategy, Fine Chemicals, Biopharmaceuticals, Manufacturing, Medical Devices and Agrochemicals