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Guidance for the safe management of hazardous medicinal products at work
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Guidance for the safe management of hazardous medicinal products at work

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For the purposes of this guide, hazardous medicinal products (HMPs) are defined as medicinal products that contain one or more substances that meet the criteria for classification as: Carcinogenic (category 1A or 1B), Mutagenic (category 1A or 1B) or Toxic for reproduction (category 1A or 1B) in accordance with Regulation (EC) No 1272/2008 (the CLP Regulation). This includes medicinal products for both human and veterinary use. By virtue of the working definition given above, HMPs fall within the scope of Directive 2004/37/EC (the Carcinogens, Mutagens and Reprotoxic Substances Directive, CMRD). HMPs include some antineoplastics, immunosuppressants, antiviral medicines, and other. HMPs are used to treat a wide range of medical conditions including cancer treatment and rheumatology. HMPs can cause unintended effects in people other than the patients themselves, such as the workers who are exposed to them.
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ISBN 978-92-76-59099-6
DOI 10.2767/052571
Luettelonumero KE-03-22-175-EN-N
ISBN 978-92-68-02978-7
DOI 10.2767/153531
Luettelonumero KE-03-22-175-EN-C
PDF
ISSN ISBN 978-92-76-59099-6 DOI 10.2767/052571 Luettelonumero KE-03-22-175-EN-N
Paperikopio
ISSN ISBN 978-92-68-02978-7 DOI 10.2767/153531 Luettelonumero KE-03-22-175-EN-C
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