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User Testing Services

Additional Useful Information

User Testing Menu

1. User Testing Home

2. Additional Information

3. Join the Testing Panel

 

Important points to consider


The leaflet that is user tested must be 'as close as possible to the final version which patients will find in the pack', i.e. User Testing cannot be carried out on a 'text only' document* (*Reference 1). CambReg has worked with clients' own production/design departments or undertaken responsibility for the design and production of mock-up leaflets.


The 'Important information' required to use the product safely and effectively must be clearly identified. It is often the case that only the client can identify the key messages for the product.


Users must be able to find, understand and act appropriately on all the key items of information.


The exact requirements for the format and content of a User Test report and acceptable user testing strategies differ between Health Authorities. CambReg has performed tests which have been submitted to Health Authorities across Europe.

 

How can leaflets be improved?

Good practice for the writing and design of package leaflets is well established and the MHRA has published a report giving advice on this*. (*Reference 2).

 

The following are examples of problem areas we have identified prior to and during the testing process:

 

Problems with design and layout:

  • Inappropriate use of colour

  • Text too small

  • Information which is perceived to be in the 'wrong section' by users

  • Insufficient differentiation between headings and body text

  • Inappropriate use of text features for emphasis e.g. italics, uppercase, underlining etc.

  • Text too dense, not enough bullet points.

Problems with text:

  • Overuse of technical language and product name

  • Side effect information presented in the wrong order and without frequency indicators
  • Lack of clear advice on what action to take and when, especially in the 'what to do if you forget to take' section

  • Indirect language

  • No reference to availability of different formats

*References
1. Additional Q’s and A’s in relation to the new legal requirement to undertake consultation with target patient groups (Compliance with article 59(3) of Council Directive 2001/83/EC) (June 06)

2. Always Read the Leaflet (July 05)


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