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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR

Clinical Trial Supply Forum 2018

Clinical Trial Supply Forum 2018

22-24 January 2018
London, UK

In the constantly changing environment of Clinical Trial Supply, cost efficiency, end to end visibility, logistics and managing complex pipelines are STILL crucial elements that need addressing!

Never before have you seen a forum that is this interactive and faces these immense challenges head on, with interactive SWOT analysis, live polls, panel debates, round table discussions, hands-on workshops and exclusive case studies.  If there is ONE Clinical Trial Supply onference that you should choose for 2018 – this is it!

Optimising your clinical trial supply chain is not the only consideration when it comes to innovation and keeping ahead in the market! Have you thought about unifying platforms in your management strategy? Do you have the correct drug supply labeling solutions? Have you truly managed to forecast your complex pipelines accurately in the last 12 months?

Join us next year to learn exactly where the pitfalls are in YOUR clinical trial supply chain, and determine - through small interactive sessions and expert case studies- how to get to grips with every aspect of your clinical trial supply.

Pharma IQ, enquire@iqpc.co.uk, +44 (0)207 368 9300
http://bit.ly/2fYwQQ8

phone +44 (0) 207 936 6948
email enquire@iqpc.co.uk
web bit.ly/2fYwQQ8
email London, UK
 
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Industry Events

14th Annual Biomarkers & Immuno-Oncology World Congress

11-13 June 2018, Westin Boston Waterfront, Boston, Massachusetts

The Biomarkers and Immuno-Oncology World Congress brings together a unique and international mix of large and medium pharmaceutical, biotech and diagnostics companies, leading universities and clinical research institutions, government and national labs, CROs, emerging companies and tool providers—making the Congress a perfect meeting-place to share experience, foster collaborations across industry and academia, and evaluate emerging technologies.
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White Papers

Conveying Medical Guidance in Clinical Trials – A Survey

Europital Medical Consultancy

With the incremental demand for proactive safety surveillance throughout the conduct of clinical trials, the role of Medical Management is at the fore in ensuring the safety and wellbeing of the participants. The complex responsibilities of a Medical Monitor (MM) starts from the design and development phase, through to study close out. Understanding the principle behind the protocol and the prospective medical solution the study would deliver forms the bloodline for the MM role. Often, the MM is the face of contact for both the site personnel and the study team members with regard to medical, safety and scientific issues within the project. When it comes to medical guidance, the communication channel used to deliver solutions contributes to a large extent in effectively managing decisive situations. Our previous study on acquiring medical guidance from an operations team perspective revealed that e-mails were the most used communication method (see the article, 'Talking Points', in ICT November 2014). In our efforts to further strengthen the mode of medical guidance delivery, we designed a survey to study the existing trend and constraints in this communication chain management, as outlined here.
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News and Press Releases

Recipharm and Laccure agree commercial collaboration


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