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LEXQARA is an active consulting firm specializing in quality assurance and regulatory affairs for the medical device industry. The company offers expertise to support medical device manufacturers with compliance, quality management systems, post-market surveillance plans and reports, risk management documentation, audit checklists, and other regulatory requirements. With over 15 years of experience in the field and a cumulative 20 years among its team members, LEXQARA focuses on simplifying complex regulatory processes by providing templates, procedures, training materials ("LEX ebooks"), and direct consulting services to streamline daily operations for QA/RA professionals[2][7].
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