Ensures GE Healthcare Europe – EAGM - India is compliant with applicable regional medical device regulations such as the U.S. Food and Drug Administration, EU Competent Authorities, EU Directives and other international regulations.

Vice President Quality & Regulatory Affairs Europe - EAGM - India at GE Healthcare @ Ensures GE Healthcare Europe – EAGM - India is compliant with applicable regional medical device regulations such as the U.S. Food and Drug Administration, EU Competent Authorities, EU Directives and other international regulations. From May 2014 to Present (1 year 8 months) Paris Area, FranceVice President Quality & Regulatory Affairs, Europe @ Ensures GE Healthcare Europe is compliant with applicable regional medical device regulations such as the U.S. Food and Drug Administration, EU Competent Authorities, EU Directives and other international regulations. From October 2011 to May 2014 (2 years 8 months) Paris Area, FranceVP of Quality & Regulatory Philips Healthcare @ From March 2009 to October 2011 (2 years 8 months) Senior Director of Clinical & Regulatory Affairs @ •Authorized European Representative for GMD in Europe. •Responsible for all the regulatory activities for GMD Europe sa/nv •Making sure we comply with all the applicable EU medical device directives when developing and introducing a new GMD product in the market. •For Non-EU countries making sure that we comply with their local laws and product registration. From May 2007 to March 2009 (1 year 11 months) Senior Director of Clinical & Regulatory Affairs @ From April 1998 to May 2007 (9 years 2 months) Clinical Coordinator Emerging Markets @ From April 1996 to April 1998 (2 years 1 month) Tachycardia Clinical Engineer II @ From February 1992 to April 1996 (4 years 3 months)

Bachelor, Nursing @ PHIV From 1983 to 1986 Heilig Kruis College MaaseikHeilig Kruis College MaaseikHeilig Kruis College Maaseik Daniel Verstappen is skilled in: Medical Devices, FDA, ISO 13485, Regulatory Affairs, ISO 14971, Quality Assurance, CAPA, Quality System, Clinical Trials, Clinical Research, Design Control, Regulatory Submissions, V&V, Cardiology, Validation