Clinical Trial Logistics 2015
May 20 - 21, 2015
伦敦 , 英国
Over 100 attendees representing worlds leading Pharmaceutical and Biotech companies will meet in London to discuss the latest development in clinical trial supply and logistics. The 2 days will feature informative, scientific and business development presentations including round table discussions, interactive workshops, networking sessions and ground breaking case studies as addressing this rapidly growing global market which is predicted reach $14.3bn by 2017.
The conference will focus on assessing the distribution and a risk based approach to develop and manage a coherent global supply chain. With a demand to assess and analyse the regulatory developments, this conference will focus on GCP, GMP and the qualification and validation of products through their life cycle. Attendees will gain understanding in the quality assurance aspect of the clinical trial logistics procedure in addition to the partnerships between CROs and discuss the hurdles that could be faced, alongside the opportunities that are arising.
BUSINESS BENEFITS FOR 2015:
. BUILD AND ENHANCE your understanding of integrating temperature tracking at the site, analyse how data is coming into the system, review temperature monitoring of shipments, and the use of electronic labels
. ASSESS how to cut costs in clinical trial supply logistics with our INTERACTIVE ROUND TABLE DISCUSSIONS
. GAIN insights from our KOLs on how to maintain an efficient supply chain and hear CASE STUDIES from leading pharmaceutical companies and CROs on planning and forecasting for clinical trials to ensure you are working together to build a robust partnership
. DEVELOP an understanding of the regulatory, GCP & GMP requirements to control the qualification and validation of products through their life cycle
. ASSESS the globalisation of clinical trial logistics and review how companies are maintaining their their standards of quality in emerging countries with a PANEL DISCUSSION
The conference will focus on assessing the distribution and a risk based approach to develop and manage a coherent global supply chain. With a demand to assess and analyse the regulatory developments, this conference will focus on GCP, GMP and the qualification and validation of products through their life cycle. Attendees will gain understanding in the quality assurance aspect of the clinical trial logistics procedure in addition to the partnerships between CROs and discuss the hurdles that could be faced, alongside the opportunities that are arising.
BUSINESS BENEFITS FOR 2015:
. BUILD AND ENHANCE your understanding of integrating temperature tracking at the site, analyse how data is coming into the system, review temperature monitoring of shipments, and the use of electronic labels
. ASSESS how to cut costs in clinical trial supply logistics with our INTERACTIVE ROUND TABLE DISCUSSIONS
. GAIN insights from our KOLs on how to maintain an efficient supply chain and hear CASE STUDIES from leading pharmaceutical companies and CROs on planning and forecasting for clinical trials to ensure you are working together to build a robust partnership
. DEVELOP an understanding of the regulatory, GCP & GMP requirements to control the qualification and validation of products through their life cycle
. ASSESS the globalisation of clinical trial logistics and review how companies are maintaining their their standards of quality in emerging countries with a PANEL DISCUSSION
组织者
SMi Group Ltd
2nd Floor South, Harling House
47-51 Great Suffolk Street
London
SE1 0BS
United Kingdom
+44 (0) 20 7827 6000