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This document proposes the inclusion of misoprostol as a treatment for incomplete abortion and miscarriage based on its safety, efficacy, and public health relevance. It provides evidence supporting
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How to fill out 17th Expert Committee on the Selection and Use of Essential Medicines

01
Read the guidelines provided by the World Health Organization (WHO) regarding the Expert Committee.
02
Gather all necessary documentation and evidence related to essential medicines.
03
Organize the data according to the categories specified in the guidelines.
04
Fill out the application form with accurate information about the essential medications.
05
Submit the completed application form along with supporting documents before the deadline.
06
Follow up for any additional information or clarification requested by the committee.

Who needs 17th Expert Committee on the Selection and Use of Essential Medicines?

01
Healthcare professionals involved in prescribing or recommending essential medicines.
02
Pharmaceutical companies looking to have their products recognized as essential.
03
National health authorities aiming to improve their essential medicines list.
04
Researchers and policymakers focusing on medication accessibility and public health.
05
Organizations working on health interventions and programs in low-income settings.
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People Also Ask about

The Use of Medicines Committee (UMC) is a multi-disciplinary team that is responsible for overseeing all medicines management practice within UCLH, including the Medicines Formulary.
The WHO Model List of Essential Medicines (a.k.a. Essential Medicines List or EML), published by the World Health Organization (WHO), contains the medications considered to be most effective and safe to meet the most important needs in a health system.
Medicines Act The Act ensures that the medicines and products used in New Zealand are safe and effective.
Essential medicines are those that satisfy the priority health care needs of the population. They are selected with due regard to public health relevance, evidence on efficacy and safety, and comparative cost-effectiveness.
The Use of Medicines Committee oversees medicines management issues including the trust formulary (a list of medicines that are approved for use within UCLH) and the assessment of new drugs.
The Committee for Medicinal Products for Human Use (CHMP) is the European Medicines Agency's (EMA) committee responsible for human medicines. It plays a vital role in the authorisation of medicines in the European Union. The committee meets once a month.
The first WHO Model List of Essential Medicines was published in 1977 and included about 200 medicines. It was seen as a major revolution in public health, highlighting that some medicines are more important than others.
The PTC performs the following functions: Prevent and monitor adverse drug reactions and medication errors. Evaluate, develop, and promote drug therapy guidelines. Develops policies and procedures for handling medications, include procurement, prescribing, distribution, and administration processes.

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The 17th Expert Committee on the Selection and Use of Essential Medicines is a panel convened by the World Health Organization (WHO) to assess and recommend essential medicines that are necessary for a basic health care system.
Health authorities, pharmaceutical companies, and other stakeholders involved in the procurement and distribution of medicines may be required to submit their recommendations or findings to the committee.
To fill out the submission for the committee, detailed information regarding the medicine's efficacy, safety, cost-effectiveness, and relevance within the context of public health must be provided in the prescribed format specified by WHO.
The purpose of the committee is to ensure that essential medicines are selected based on solid evidence and to improve access to these medicines to meet the health needs of populations worldwide.
The information that must be reported includes the name of the medicine, its indications, dosages, side effects, alternative treatments, and data on its effectiveness and safety, along with economic evaluations.
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