Lachman Consultant Services, Inc. (Lachman Consultants), a leading provider of expert compliance, regulatory affairs and technical services to life sciences clients worldwide, will be a prominent participant at the second annual MedtecLIVE 2019 conference. This year’s MedtecLIVE event will take place in Nuremberg, Germany from May 21st through May 23rd at the Exhibition Center Nuremberg. Attendees are invited to visit with Lachman Consultants in Exhibitor Hall 10.0 at Booth #128.
With its growing presence in Europe and offering deep medical device expertise and experience, the Lachman Consultants team will be on hand to meet and discuss its wide range of consulting services for areas that include medical products, IT, materials and components, processes and mechanical engineering and manufacturing, as well as testing and validation. Of particular interest to attendees who visit with Lachman Consultants is their proven expertise and broad range of consultative services for combination products such as auto injectors, pre-filled syringes, patch delivery systems and many others.
Well-versed and accomplished in this rapidly growing life sciences sector, Lachman Consultants provides clients with compliance support that includes due diligence review, general auditing, quality assessment remediation work for 483 or warning letters, as well as design history file building and documentation. Company executives will be on site to discuss the firm’s full menu of regulatory services that include traditional 510k, Genovo filing under 510k and premarket clearance. They will also be detailing Lachman Consultants’ past experience in areas that include validation review work and complete support for systems and data in preparation for application.
Dave Lonza, Head of EU for Lachman Consultants will be participating at this year’s event along with other executives and senior staff officials. David Lonza heads the firm’s office in Luzern, Switzerland and oversees Lachman’s European-based resources. “We’re excited to be attending MedtecLIVE 2019, as our industry is growing and innovating at such a rapid pace,” Lonza states. “This is one of our industry’s premier events and we look forward to connecting with the many returning attendees that made last year’s inaugural event so successful.”
Using a dedicated, single-point-of-contact approach, multi-disciplinary groups of accomplished FDA and industry experts are assembled from Lachman Consultants’ Compliance, Regulatory, and Science and Technology Practice Groups to evaluate, advise, strategize, create protocols, and help fulfill requirements wherever needed. These teams are selected and assigned according to each client’s specific set of objectives, needs, and circumstances.
“Europe represents a significant growth region for our company,” adds Lonza. “With our growing presence in this part of the world, European-based clients appreciate the regional adjacency, cultural familiarity, and most importantly, our expertise in global regulatory and compliance requirements.”
This second edition of the MedtecLIVE 2019 conference will provide a distinct focus on the entire supply chain, from prototypes through production as well as post-manufacturing processes. At the concurrent MedTech Summit 2019 in Nuremberg, medical technology will intersect with innovation and leading-edge technologies.