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Stability challenges Part II: Assuring the stability of medicines from manufacture to clinical use

11 December 2014, London, United Kingdom


Introduction
The focus of this symposium is to examine best practice during the distribution and storage of medicines, to ensure correct storage conditions are maintained and to ensure the quality of the medicine is maintained during use in the clinic or by the patient. The generation of data to support temperature excursions and to demonstrate in-use stability will be explored.

This meeting will be of interest to those engaged in Quality Control and Quality Assurance, pharmaceutical development and regulatory affairs in the Pharmaceutical Industry, NHS manufacturing units, CMOs and academia.

This meeting builds on the successful Meeting Stability Challenges JPAG meeting held in 2013.

Registration at 9.30 a.m.; symposium starts at 10.00 a.m

To register please choose 'book now' in the top right corner of the page.


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Speakers
  • Mark Santillo South Devon Healthcare NHS Foundation Trust, United Kingdom
  • Eric Behets Principal Scientist, Baxter Healthcare R&D, Alliance Park, Belgium
  • Kerry Bradford Intertek-Melbourn Scientific, United Kingdom
  • Paul O’Connor Almac Clinical Services, United Kingdom
  • David Clapham GSK, United Kingdom
  • Stuart Jackson, Head of Quality, The Specials Laboratory, United Kingdom

Venue
The UUÂãÁÄÖ±²¥ of Chemistry

Science Room, The UUÂãÁÄÖ±²¥ of Chemistry, Burlington House, Piccadilly, London, W1J 0BA, United Kingdom

Useful links

Organised by
Joint Pharmaceutical Analysis Group
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