Easily Delete Symbols into the Health Care Directive

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How to Delete Symbols into the Health Care Directive

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hi Im Neil winger Im a general interest to primary care doc and also I work with the UCLA health ethics center and Im here to talk with you about advance directives whats an advance directive its a legal document that allows you to indicate what kinds of things you would want done if you couldnt make decisions for yourself now why would that happen we know that optimally doctors and patients work together in shared decision-making to make sure that the kinds of treatments that patients receive reflect what patients would want but under unusual circumstances patients cant talk with their physicians about what they would want perhaps theyre too sick or perhaps something horrible happened and theyre not awake under those circumstances who would you want the doctors to turn to to help make decisions for you maybe its a spouse perhaps a sibling maybe even a friend and if it is a friend with the doctors know to turn to that person probably not its for those reasons that people nee

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What is European Directive 2001 83?

(1) 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, codified and consolidated in a single text the texts of Community legislation on medicinal products for human use, in the interests of clarity and rationalisation

What is Article 52 of Directive 2001 83 EC?

[F1Article 52a Importers, manufacturers and distributors of active substances who are established in the Union shall register their activity with the competent authority of the Member State in which they are established.

What is Article 51 of 2001 83?

The duties of the Qualified Person (QP) are fully described in Article 51 of Directive 2001/83/EC, and can be summarized as follows: a) For medicinal products manufactured within the EC a QP ensures that pro- duction and testing is in ance with the directives and the marketing authorization.

What are the 3 safety features of the EU falsified medication Directive?

Legal framework The Falsified Medicines Directive Obligatory safety features a unique identifier and an anti-tampering device - on the outer packaging of medicines. A common, EU-wide logo to identify legal online pharmacies. Tougher rules on import of active pharmaceutical ingredients.

What regulation is Directive 2001 83 EC?

1. No medicinal product may be placed on the market of a Member State unless a marketing authorization has been issued by the competent authorities of that Member State in ance with this Directive or an authorization has been granted in ance with Regulation (EEC) No 2309/93.

What is Article 51 of Directive 2001 83?

Article 51 (1) (b) of Directive 2001/83/EC on the Community code provides that ATMPs imported from a third country must be re-tested upon importation by the qualified person for batch control.

What is Article 46 of the Directive 2001 83 EC?

[F1Article 46b 1. Member States shall take appropriate measures to ensure that the manufacture, import and distribution on their territory of active substances, including active substances that are intended for export, comply with good manufacturing practice and good distribution practices for active substances.

What is Article 47 of the Directive 2001 83 EC?

Article 47 [F1The Commission is empowered to adopt delegated acts in ance with Article 121a in order to supplement this Directive by specifying the principles and guidelines of good manufacturing practices for medicinal products referred to in Article 46(f).]

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