We make complex things easier - all the way from idea to market - with focus on the Life Science industry providing complete solutions in all aspects of regulatory compliance. Key2Compliance® is a full-service partner that offers complete solutions in all aspects of consultancy and training needs when it comes to: • Medica Device Quality Assurance: Quality system, GXP, technical files, inspections, audits, PRRC responsibility • Regulatory Affairs: Documentation and CE markings, FDA approvals and registrations in the rest of the world • Biological Evaluations and Toxicology: Biological evaluation, material documentation, recommendations, reports and more • Clinical Development: Clinical evaluations, prospective clinical studies, and post marketing studies • Pharma Quality Assurance: Pharma Quality Assurance: GCP, GVP, GMP, GDP and GLP, Quality system, audits, QA-manager etc. • Training and Courses: World-leading training for Life Science industry when it comes to compliance training: in-house, public, on-site, on-location, online, on-demand, printed matters, board games, online documentation library, online testing and eBooks Key2Compliance® - Rely on us! Symbioteq Kvalitet AB and Key2Compliance® were founded as two independent companies 1994 and 1995. Symbioteq focused on consulting in Regulatory and Quality for medical devices and Key2Compliance® soon became a leading company in Training and Education in the field of Current Good Manufacturing Practice (cGMP). After several years of cooperation, the two companies merged in 2020 and formed a joint company called Key2Compliance®, a company within the Symbioteq group. With our strengthened offering, it is our ambition that Key2Compliance® will become the foremost partner for pharmaceutical and medical device companies, not only in Sweden but at an international level. Key2Compliance® has offices in Stockholm, Lund, Gothenburg and Copenhagen.