Lothar Krings

Lothar Krings currently serves as a seasoned Business Consultant at Freelance, where he leverages over 18 years of specialized expertise in the development, manufacturing, and regulatory approval of complex implantable medical devices. His role involves providing strategic guidance and hands-on support to medical device companies navigating the intricate landscape of design validation, quality management systems, and compliance with international standards such as FDA and CE regulations. Lothar’s deep understanding of the technical and regulatory nuances of Class III implantable devices—ranging from Cardiac Rhythm Management systems to Brain-Computer Interfaces—enables him to streamline product development processes, mitigate risks, and accelerate time-to-market.

At Freelance, Lothar is instrumental in managing cross-functional teams and fostering collaboration across distributed R&D units and manufacturing networks. His expertise in managing complex supply chains and coordinating international teams across diverse cultures and languages ensures seamless project execution from concept to commercialization. He also offers invaluable insights into managing intellectual property, safeguarding innovations while maintaining compliance with global regulatory frameworks.

Key projects under his leadership often involve guiding startups and established medical device manufacturers through the rigorous pathways of FDA and CE approval, optimizing quality assurance protocols, and establishing robust manufacturing processes for high-risk implantable devices. His comprehensive approach combines project management, regulatory strategy, and technical expertise, making him a trusted partner for organizations aiming to bring innovative implantable devices to market efficiently and safely. Lothar’s industry-specific knowledge and hands-on experience position him as a vital resource in advancing the development of life-changing medical technologies.