This includes the outer and inner packaging of the medicine, and the printed package leaflet. Contact your EMA account manager to learn more. Learn more about how the pharmaceutical industry is actively involved in the work of the Agency. The materials used are of pharmaceutical grade, FDA and food contact approved. 2. The European Medicines Agency operates a checking process of the printed materials used in the packaging and labelling of centrally authorised medicines.. Pharmaceutical Industry With almost a century of experience, EMA Pharmaceuticals is a leader in the manufacturing of sealing solutions for pharmaceutical applications. Health, representing the Agency's mission to pr… This is unlikely in a commercial context if the EMA logo is used in conjunction with a company's own logo, name or trade mark.Please note that EMA will pursue cases of abuse and fraudulent use of the logo.EMA will not rebrand the thousands of legacy documents published on the EMA website before 8 December 2009. EMA Pharmaceuticals provides a large range of seals, each of which conform to the pharmaceutical container standards. After the health crisis linked to COVID-19, EMA Pharma received historic orders from the large group GSK (British group) for the manufacture of capsules to crimp the bottles of future vaccines.With almost a century of experience, EMA Pharmaceuticals is a leader in the manufacturing of sealing solutions for pharmaceutical applications.Solely dedicated to the pharmaceutical industry, we currently serve more than 170 production sites of injectable medicine across the world.EMA Pharmaceuticals presents SMARTSEAL, a powerful covert anti-counterfeiting feature, enabling the easy track & trace of the individual container through RFID technology.SMARTSEAL allows fast and effective inventory control, facilitates product recalls and enhances ultimately patent safety. List item. The aim of this checking process is to improve the quality of the printed materials that patients and healthcare workers receive with a medicine. The EMA logo is a stylised representation of a pestle and mortar - one of the most ancient and universally recognised images associated with medicines:The logo should be used in its entirety without distorting, modifying or separating its component elements.Permission to use the EMA logo does not confer on those to whom it is granted any right of exclusive use, nor does it allow them to appropriate the logo, either by registration or any other means.The Agency will examine requests to use the EMA logo individually to determine whether they satisfy the above criteria. The European Medicines Agency (EMA) has launched its third communication perception survey . EMA Pharmaceuticals presente SMARTSEAL, une puissante fonction secrète anti-contrefaçon, qui permet de suivre et de tracer facilement le conteneur grâce à la technologie RFID. Science, representing the scientific expertise that guides the EMA in its regulatory decision-making.

Medicines, representing EMA's focus on assessing and monitoring medicines to ensure their quality, safety and efficacy. ... EMA and the Heads of Medicines Agencies have developed a joint strategy to tackle shared challenges for the European medicines regulatory network. The United Kingdom (UK) withdrew from the European Union (EU) on 31 January 2020 and is no longer an EU Member State. The EMA logo is a stylised representation of a pestle and mortar - one of the most ancient and universally recognised images associated with medicines: The straplinein the EMA logo represents the three pillars the Agency's work is based on: 1. SMARTSEAL permet un contrôle rapide et efficace des stocks, facilite les rappels de produits et améliore en fin de compte la sécurité des brevets. The different cap designs are available with a large choice of colors of aluminum and polypropylene parts. If the site still contains content that does not yet reflect the withdrawal of the UK from the EU, this is unintentional and will be addressed.

The draft document is available for public consultation until 4 September 2020.

The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of medicinal products.Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA).. Solely dedicated to the pharmaceutical industry, we currently serve more than 170 production sites … Communication@EMA – how are we doing?

They will continue to bear the former EMA logo.

EMA is in the process of making appropriate changes to this website. 3. They are suitable for sterilization by steam, irradiation, ethylene oxide