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23 gen 2019 · Guidance on the Administration of Medicines in Healthcare Settings. E N D O R S E D BY. Introduction. This professional guidance has been co-produced by the Royal Pharmaceutical Society (RPS) and Royal College of Nursing (RCN) and provides principles-based guidance to ensure the safe administration of medicines by healthcare professionals.
Guideline for the pharmacological treatment of hypertension in adults. Geneva: World Health Organization; 2021. Licence: CC BY-NC-SA 3.0 IGO. Cataloguing-in-Publication (CIP) data. CIP data are available at http://apps.who.int/iris. Sales, rights and licensing. To purchase WHO publications, see http://apps.who.int/bookorders.
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The compilation of European Commission and Agency guidelines contains: all valid guidelines originally published in volume 3; all valid guidelines published by the Agency since 1995; these guidelines' revisions and supplements. Depending on each guideline's status, one or more of the following documents are available: concept paper; draft ...
for vaccine administration. The legislation supporting this however, would apply to the administration of other prescription only medicines (POMs) by unregistered staff and therefore may be useful in other contexts. Administration The administration of medicines in a health care setting must be done in accordance with a
23 ago 2023 · A medication administration route is often classified by the location at which the drug is administered, such as oral or intravenous. The choice of routes in which the medication is given depends not only on convenience and compliance but also on the drug’s pharmacokinetics and pharmacodynamic profile.
- Jean Kim, Orlando De Jesus
- 2023/08/23
- 2021
This ICH GCP Guideline Integrated Addendum provides a unified standard for the European Union, Japan, the United States, Canada, and Switzerland to facilitate the mutual acceptance of data from clinical trials by the regulatory authorities in these jurisdictions.
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Guidance documents represent the Agency's current thinking on a particular subject. They do not create or confer any rights for or on any person and do not operate to bind FDA or the public. An alternative approach may be used if such approach satisfies the requirements of the applicable statute, regulations, or both. For information on a specific ...
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