12 - 13 October, 2016 | Hilton London Olympia , London, United Kingdom

Stephen Buss

Director of Scientific Affairs
Vape Compliance

11:20 Creating a Masterfile of all the data needed to apply for licence: How realistic is the concept of standardisation?

  • How far are we from this? What areas would we standardise?
  • What can we do if we bring our strengths together?
  • Harmonising standards between Europe and overseas to ease trade between different countries
  • Creating a master file – is that possible? What are the plans?
  • Creating a database of studies already done in the space, so people don’t need to do studies again
  • Testing methodology and properties that are common and that can be used to apply for PMTA.What should these look like for everyone?
  • Standards for toxicity – how to access toxicity?

10:40 Developing and working within the ISO standards: What do you need to have to be compliant?

  • Examining how ISO standards could benefit your organisation to evaluate the benefits of obtaining licence
  • Understanding the analytical requirements around ISO 9001
  • Obtaining ISO standards through accreditation: Looking at the preparation and the application process
  • Installing core management strategies to drive the business forward through continuous improvement
  • Developing a specific standard that will enable e-cig brands to keep their boutique approach
  • Examining methods for operating effectively within the current GMP standards

Check out the incredible speaker line-up to see who will be joining Stephen.

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