With more clinical trials being held in Asia than ever before, your clinical trial supply system needs to become increasingly sophisticated in order to cope with importation and exportation guidelines, local regulations, packaging and labelling requirements and temperature-controlled storage. Clinical Trial Supply Asia offers you the chance to get critical input on overcoming the key challenges of clinicalsupply chain in the region. Through top level strategic insights and practical case ...
This joint programme will offer the opportunity for intensive discussion among stakeholders in different topics relevant for paediatric medicines. It will address visions, daily challenges and ways forward in paediatric drug development. Conference objectives are to: update participants how to deal with paediatric regulatory requirements, scientific and operational challenges, exchange experiences with regulatory authorities, academia and industry and discuss visions, daily challenges and ...
Improve drafting and negotiation skills by attending this specifically designed seminar which tackles the issues that can arise when handling clinical trial agreements (CTAs). Analyse 'typical' clauses and ensure that the agreement offers you the best deal Understand the key differences between European and US CTAs Assess agreements from different perspectives (e.g. from the perspective of the sponsors, universities, and hospitals) enabling you to negotiate more effectively Compare experiences ...
