About myself:My heart's beating for two different worlds: Product Development and Regulatory Affairs. I am both a passionate engineer and a regulatory geek. This enables me to easily navigate between regulatory paperwork, innovative product concepts and fast paced R&D projects. So I definitely know how to connect the dots from early design prototypes to the final page of a regulatory submission.My work experience covers more than 15 years in multiple positions from demanding coordinational tasks like Project Management, Project Coaching, M&A Integrations, Regulatory Affairs Management down to really profound nerdy subject matters tasks like biological evaluations, toxicological risk assessments, clinical evaluations, clinical trial management, submission compilation and technical documentation creation or remediation.​Just give me a task and I get it done – Straight Forward.----------------------------About my company:Our consultants support you in the areas of regulatory affairs, project management and quality management for medical devices and healthcare products.We are your partner for a successful product development, a fast market access and an efficient quality management system.Our passion, expertise, integrity, commitment, heart & soul for your safe and effective products.Satisfied customers / StraightForward.----------------------------Check out our team and some client testimonials athttps://www.straightforward-consulting.com/referenzen/