Conference · Berlin, Germany
Clinical Trials Supply Chain 2013
Chemistry · Management · Pharmaceuticals
Key numbers
- Editions on record
- 2first in 2013
About Clinical Trials Supply Chain
The key challenge clinical trial supply chain managers face in global distribution is ensuring that supplies arrive at the trial sites on time and in good condition.
Effective distribution require:
• an understanding of regulations in the country of origin as well as in trial countries
• qualified suppliers and storage infrastructure
• and control of supply temperature and conditions for the duration of delivery
Regulatory support is a critical aspect of clinical trial supply distribution, requiring the creation and control of essential documents and activities to ensure a seamless supply of clinical materials. Therefore our two-day event will devote three workshop sessions to the impact of EU guidelines on clinical supplies (GDP/GMP/GCP). Attendees will also learn how to maximize the efficiency and ensure the safety of clinical supplies, gain insight into packaging & labeling solutions, temperature-controlled distribution and much more!
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2015 | 29–30 Sep 2015 | Novotel Berlin Am Tiergarten Berlin, Germany | — | — |
| 2013 | 20–21 Nov 2013 | Eurostars Berlin Hotel Berlin, Germany | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.