ISO 13485 Certification, PMA, Regulatory & CE Mark Consultants, 510k Consulting, European Authorized Representative & Clinical Trials - Methodizeinc Methodize Inc. is a consulting and training firm specializing in regulatory, clinical and quality services, We have been helping companies all over the world in bringing medical devices. http://www.methodizeinc.com/ Methodize Inc http://www.methodizeinc.com/images/methodize_logo.gif http://www.methodizeinc.com/ http://www.methodizeinc.com/our_expertise.html ISO 13485, ISO 9001, Regulatory Submissions IDE, 510k, PMA, Clinical Trials International, FDA Help, Consulting & Quality System Requirements We have been helping companies all over the world in bringing medical devices, Regulatory Submissions, FDA Help & In-Vitro Diagnostics products to market, Methodize is the one to call. http://www.methodizeinc.com/our_expertise.html http://www.methodizeinc.com/about_us.html Regulatory Submissions IDE, 510k, PMA, Clinical Trials US & South America - About Methodize Inc Methodize Inc., is a consulting and contracting firm offer a full range of contract research organization, biological safety assessment, seminars, books & productivity tools services. http://www.methodizeinc.com/about_us.html http://www.methodizeinc.com/partners.html Methodize Inc. Partners - Internal Quality Audit Help, Clinical Trials, ISO 13485 & FDA Quality System Requirements Our mission is to provide our clients knowledge, integrity & services to successfully take their products from an idea on a napkin to market. We provide efficient and effective solutions. http://www.methodizeinc.com/partners.html http://www.methodizeinc.com/sitemap.html ISO 9001 & 13485 Certification, CE Mark, Authorized Representative, Clinical Trials EU, US & International - Methodizeinc With over 35 years of combined Regulatory, Quality and Clinical services we have been helping companies all over the world in bringing medical devices and In-Vitro Diagnostics products to market. http://www.methodizeinc.com/sitemap.html http://www.methodizeinc.com/articles.html ISO Quality Certification, ISO 9001 & 13485, CE mark, Authorized European Representative, Clinical Trials US - Methodizeinc Methodizeinc providing Regulatory, Quality and Clinical services with over 35 years, we have been helping companies all over the world in bringing medical devices and In-Vitro Diagnostics products to market. http://www.methodizeinc.com/articles.html http://www.methodizeinc.com/regulatory-consulting.html Medical Device Regulatory Consulting, 510(k), CRO, IDE & PMA Consulting - Methodizeinc Our services also ensure that post market compliance is maintained throughout labeling advice and compliance with the applicable regulations. http://www.methodizeinc.com/regulatory-consulting.html http://www.methodizeinc.com/submitting-510-application.html Submitting a 510(k) Application - Methodizeinc Companies that need to submit a 510(k) application are manufacturers or importers of some Class 1 and Class 3, and most Class 2 medical devices. http://www.methodizeinc.com/submitting-510-application.html