Comparative User Testing of Australian and UK Over-the-Counter Labels and Leaflets for Diclofenac

Author:

Tong Vivien,Raynor David K.,Aslani Parisa

Funder

The University of Sydney

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Reference42 articles.

1. Medicines and Healthcare products Regulatory Agency. Medicines: reclassify your product. https://www.gov.uk/guidance/medicines-reclassify-your-product. Published December 18, 2014. Accessed May 6, 2016.

2. Australian Government Department of Health Therapeutic Goods Administration. Poisons Standard July 2016: Schedule 1—Standard for the Uniform Scheduling of Medicines and Poisons No. 13, Australia. https://www.legislation.gov.au/Details/F2016L01071. Accessed September 24, 2016.

3. Bolaños H. Responsible self-medication in Latin America. Drug Inf J. 2005;39:99–107.

4. European Commission. Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use. Brussels: European Commission; 2001.

5. Australian Government Department of Health Therapeutic Goods Administration. Therapeutic Goods Order No. 69—General requirements for labels for medicines. https://www.legislation.gov.au/Details/F2014C00926. Accessed September 24, 2016.

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