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19 20 21 22 * BORDERLINES BETWEEN MEDICINES AND FOOD
 23 * REGULATORY AFFAIRS IN THE MIDDLE EAST
* US PATENT PRACTICE
* PRACTICAL INTRODUCTION TO INTERNATIONAL PATENT LAW AND PRACTICE
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26 27 28 29 30 * CRO / VENDOR MANAGEMENT IN THE PHARMACEUTICAL INDUSTRY
 31 * THE NEW ROLE OF THE QUALIFIED PERSON UNDER THE MEDICAL DEVICES DIRECTIVES
  
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USABILITY
ENGINEERING IN DRUG
DELIVERY PRODUCTS

Pre-Conference Workshop

Conference Date: 22 May 2012
Conference Ref: N5-8112
Fee: £599 + VAT
Venue: The Cavendish Hotel, London

DISCOUNTED PRICE IF BOOKED TOGETHER WITH PRE-FILLED SYRINGES CONFERENCE ON 23 & 24 MAY

TOPICS TO BE COVERED:

  • What are human factors and usability?
  • Overview of current standards and guidance
  • Requirements for medical products and application to drug delivery products
  • Integration into drug delivery development projects ~ Timing and implementation
  • The relationship and combination with risk management
  • Impact on Development of Labelling, Instructions for use and training programme and aids
  • Roles of  Human Factors Experts/Companies
  • Usability and Software
  • Differences between USA vs EU requirements

If you have any further questions please click here  to contact Andrea James

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