PPT-Falsified Medicine Directive

Nicholas Falzon PRIMA President Definition of a Falsified Medicine According to the WHO a Falsified Medicine is a Medical product that deliberatelyfraudulently misrepresent their identity composition or source. Medicines are now the second largest categor y of falsified items imported into Europe ZKHUHDV57347WKH57347GLGQ57526W57347ZDUUDQW57347D57347VHSDUDWH57347FDWHJRU57347LQ 004 because numbers were so low The chart below displays an increasing trend in i UNDERSTANDING. AN IDEA IS ABLE TO BE . PROVEN. WRONG.. IF YOU. PROVE . SOMETHING WRONG, YOU HAVE “FALSIFIED” IT.. YOU . WOULD ONLY NEED TO MAKE AS LITTLE AS ONE OBSERVATION TO FALSIFY IT.. “FALSIFIABLE” MEANS:. PT. Falsified Medicines. R. esponding . E. ffectively to the . P. roduction of and . T. rafficking in Falsified Medicines. Law Enforcement Training on Falsified Medicines. Accra (Ghana), October 6, 2015. Dr. P. V. . Appaji. , . M.Pharm. , . Ph.D. Director General,. PHARMACEUTICALS EXPORT PROMOTION COUNCIL OF INDIA. Hyderabad. Email: dg@pharmexcil.com. Presentation by. CONTENTS. Which are EU Countries?. P. aul . N. e. w. t. on. . History . Definitions. Legal aspects. Impact . –. . Patient . o. utcome. Impact . –. Economy and Society. Impact . –. Resistance. Impact - Trials. A forgotten history……. . Leyla Hannbeck . MRPharmS, MBA, MSc, MA. NPA Chief Pharmacist and Director of Pharmacy. Falsified medicines: the facts. Falsified medicines may:. Be fraudulently mislabelled. Contain low quality ingredients. [INSERT DATE HERE]. [NAME OF PRESENTER]. [TITLE OF PRESENTER]. [COMPANY NAME]. Falsified medicines – a real problem. 2. The Pharmaceutical Journal, 5. th. June 2014. Why we need a Directive . Falsified products still being found in legitimate medicines supply chain – major risk to patient safety. [INSERT DATE HERE]. [NAME OF PRESENTER]. [TITLE OF PRESENTER]. [COMPANY NAME]. Falsified medicines – a real problem. 2. The Pharmaceutical Journal, 5. th. June 2014. Why we need a Directive . Falsified products still being found in legitimate medicines supply chain – major risk to patient safety. Appaji. , . M.Pharm. , . Ph.D. Director General,. PHARMACEUTICALS EXPORT PROMOTION COUNCIL OF INDIA. Hyderabad. Email: dg@pharmexcil.com. Presentation by. CONTENTS. Which are EU Countries?. Objectives of EU Directive 2001/83/EC. [INSERT DATE HERE]. [NAME OF PRESENTER]. [TITLE OF PRESENTER]. [COMPANY NAME]. Falsified medicines – a real problem. 2. The Pharmaceutical Journal, 5. th. June 2014. Why we need a Directive . Falsified products still being found in legitimate medicines supply chain – major risk to patient safety. [INSERT DATE HERE]. [NAME OF PRESENTER]. [TITLE OF PRESENTER]. [COMPANY NAME]. 2. FMD timeline and concept. Falsified Medicines Directive (FMD) timeline. 4. 2011. 2013. 2015. 2016. 2019. 2024. Directive 2011/62/EU adopted. Scanning packs – what to look for Implementing the EU Falsified Medicines Directive in the UK [INSERT DATE HERE] [NAME OF PRESENTER] [TITLE OF PRESENTER] [COMPANY NAME] FMD – what the “right” packs look like The . HDA (formerly BAPW) . Who we are. Good Distribution Practice . HDA is a UK-wide representative trade association whose mission is to advance the interests and values of those member companies who provide . www.radhazonline.com. Introduction. All employers have a duty to assess risks arising from work undertaken and to put in place protective or preventive measures to reduce the risks they identify. These duties are a requirement of the ‘overarching’ Framework Directive (89/391/EEC) already transposed into UK law (.