Deadline for Re-Registration of Medical Devices and IVDs in the UK is 31 May 2009
Summary
London, United Kingdom, April 19, 2009 --( QFI has also published a free white paper on Amending Directive 2007/47/EC on the company website at www.qualityfirstint.com/freewhitepaper.htm.“At stake is maintaining or increasing share in the European medical devices market“, says Haroon Atchia, CEO and Technical Director of QFI.QFI provides regulatory advice, quality assurance and clinical trial services, with particular emphasis on the European, US, Japanese, Australian, Canadian and Chinese marketplaces.Consequently, for instance, all EU Authorised Representatives (EUARs) are now required to re-submit information on manufacturers and products they have registered with the MHRA, including Schedules of Products, no later than 31 May 2009.QFI has also published a free white paper on Amending Directive 2007/47/EC on the company website at www.qualityfirstint.com/freewhitepaper.htm.“At stake is maintaining or increasing share in the European medical devices market“, says Haroon Atchia, CEO and Technical Director of QFI.QFI provides regulatory advice, quality assurance and clinical trial services, with particular emphasis on the European, US, Japanese, Australian, Canadian and Chinese marketplaces.