Maetrics Initiates Research Study on MDD 2007
Maetrics has recently initiated a research study on understanding and preparations for the upcoming transition to the European Authority's MDD 2007 that is set to take effect on March 21, 2010.
After qualitative research involving professionals in the quality and regulatory functions of multiple global medical device manufacturers, Maetrics has determined a great deal of uncertainty and conflicting opinions about both the interpretation of this new directive as well as the expected impacts. This discovery has led to the instigation of a more in-depth quantitive analysis in order to provide a greater understand to our industry associates.
We are calling upon all qualified quality and regulatory personnel involved in medical device manufacturing who sell in markets guided by EU's Medical Device Directives to provide their valuable input on this pivotal change. If you meet these requirements, we invite you to participate by clicking here and providing your insights.
Upon conclusion, Maetrics will be publishing an analytical white paper that will be available to survey participants, and will be published in a top industry journal. We value the thoughts of our colleagues, and hope to provide medical manufacturers with a greater degree of clarity and direction as to the planning, implementation and ongoing management of the initiatives brought forth by MDD 2007.
Please click hereto provide your input to our research initiative on MDD 2007/47/EC (M5). You will also have the opportunity to sign up & receive a free post-analysis white-paper. If you have any further questions or thoughts, you can contact Maetrics directly. We appreciate your contribution to this research effort.
