Working group on promotion of therapeutic products

By AusBiotech
Thursday, 23 February, 2012

Key industry stakeholders, via a working group that included AusBiotech, have been debating whether or not companies, including medical device companies, should prescribe to a harmonised code of conduct to achieve TGA registration.

The working group has agreed a set of principles and AusBiotech has signed up to support them. AusBiotech is now in the process of reviewing its code of conduct to see how it may be amended to meet the spirit of the review and align with expectations from the Parliamentary Secretary for Health and Ageing, the Hon. Catherine King.

The therapeutic goods industry associations each have a self-regulatory Code of Conduct or Code of Practice, which sets the standards for companies when promoting a medicine or medical device. The Codes of Conduct/Practice include mechanisms for dealing with complaints about advertising.

In addition there is a complaints process that deals with complaints about advertising about all types of therapeutic goods where the advertising appears in the mainstream media (such as TV and radio).

The therapeutic goods industry is broadly organised around the types of products its member companies supply:

  • Prescribed medicines (medicines that you can only get with a prescription). This sector includes both companies that are researching new medicines (innovator companies) and companies that are supplying generic medicines once a patent has expired.

  • Non-prescription consumer healthcare products (including medicines you can get from a pharmacy without a script and those you can buy in a supermarket)

  • Complementary medicines and natural healthcare products (including vitamins, mineral and nutritional supplements, special purpose foods, herbal and homoeopathic medicines, aromatherapy products and natural cosmetics)

  • Medical devices and diagnostics (such as syringes and wound dressings, as well as high-technology implanted devices such as pacemakers, defibrillators, hip and other orthopaedic implants)

  • In Vitro diagnostics (instruments and test reagents for pathology tests requested by doctors as well as over-the-counter tests such as blood glucose meters for diabetes testing or home pregnancy test kits)

If you would like to make a complaint about an advertisement or other conduct by a company you will find further information about how to lodge your complaint and what you can expect from the complaints process on the websites listed below.

Where you should go to make your complaint will depend on the type of product involved and where you saw or heard the advertisement.

The Complaints Resolution Panel (CRP) deals with complaints about advertisements for any therapeutic product directed to consumers in TV, radio, the internet, newspapers, magazines, displays (except inside individual shops) and in cinemas. The CRP mailbox for complaints can be found here.

If your complaint is about an advertisement not covered by the CRP, you need to consider what type of product it is, referring to the general grouping of products listed above. Your complaint can be directed to one of the industry associations under a self-regulatory Code of Conduct/Practice. If you are unsure where to go, any of the industry associations listed below will be happy to guide you to the most appropriate person to contact:

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