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EMA urges patients to beware of potential falsified medicines sold by unregistered websites and vendors. To stay safe when buying medicines online, look out for the logo. The logo is clickable and will appear on the websites of all online medicine retailers in the EU that are registered with their national regulatory authority. Clicking on the logo will take you to the register of online retailers of the country where the retailer is established and registered, corresponding to the flag displayed on the logo. Once there, check that the retailer is listed. The national flag and the text are an integral part of the logo. A logo that displays the EU flag, for example, is not authentic. When you buy medicines from unregistered sources you are at greater risk of purchasing falsified medicines. These medicines may not have passed through the usual rigorous evaluation processes that ensure that a medicine is fit for the EU market. As a result, these medicines may not work or may be harmful. The consequences of taking falsified medicines can be serious for patients and may include:. The Directive obliges Member States to conduct and promote information campaigns on:. To support this effort, the Commission provides Member States with information and communication materials to be used as such or adapted for national campaigns. Buying medicines online. In the European Union EU , it is possible to buy medicines online. Patients should only buy medicines from online retailers registered with the national competent authorities in the EU Member States, to reduce the risk of buying sub-standard or falsified medicines. The European Commission has introduced a common logo that appears on the websites of these registered retailers. Human Veterinary Regulatory and procedural guidance. Page contents Look out for the logo Dangers of falsified medicines List of registers of online medicine retailers Legal framework Related EU legislation Related content External links Topics. Look out for the logo. Do not continue with your purchase if the retailer is not on the list. Dangers of falsified medicines. Falsified medicines may: contain ingredients of low quality or in the wrong doses; be deliberately and fraudulently mislabelled with respect to identity or source; have fake packaging, wrong ingredients, or low levels of active ingredients. The consequences of taking falsified medicines can be serious for patients and may include: the disease being untreated or treatment failure; unexpected or severe side effects; dangerous interactions with medicines the patient is already taking. List of registers of online medicine retailers. EU Member State Register of online retailers. Legal framework. By 1 July Member States have to ensure that the legal provisions on the common logo are applied in their country; national regulatory authorities in the EU are obliged to list all registered online medicine retailers in their country on their websites; all online medicines retailers registered in the EU should display the logo. The Directive obliges Member States to conduct and promote information campaigns on: the dangers of falsified medicines, the risk of medicinal products supplied illegally online, and the functioning of the common logo for online sales of medicinal products. Related content Falsified medicines. Topics Regulatory and procedural guidance. Back to top.

Items where subject is 'Pharmacy and materia medica'

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All new correspondence should be addressed to our new head office location. Please update your records accordingly. Additionally, we are currently in the process of transferring and we are committed to ensure smooth transition to avoid any inconvenience during this time. Thank you for understanding and cooperation. With the effective use of Information Technology, we have implemented a number of online services and continually working for more. Click Here to Register an account for following online services. Regulatory compliance is essential and indispensable in order to assure the safety, quality and efficacy of therapeutic goods. Guidance documents published by the Authority are meant to explain the current interpretation or policy for better understanding of the industry and. For ensuring quality therapeutic goods, a network of quality control laboratories has been established. DRAP approved products and suspect therapeutic goods are tested for their quality in accordance with best international practices. To keep the citizens safe from substandard and. The Recalled Product Index provides access to consumers, healthcare professionals, industry, hospitals and sale outlets related to the information of recalled action taken for defective therapeutic goods. The following section provides an index of recalled actions in which a public. Public consultation enables organizations to consider views and ideas from the citizens and relevant stakeholders during the development of new regulatory mechanisms, either through the enactment of new rules and policies or changes to existing ones or by the development. Moreover, we have introduced centralized Case Management System in the same portal for enhanced efficiency and transparency. DRAP ensures that every drug, medical device or cosmetic, alternative medicine and health product must have a certain standard of quality and is safe and effective for your use. See in links below how it is done and what to do in case you find a suspect therapeutic good.

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