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Morningside’s Life Sciences translation services division—certified to the latest ISO 9001, ISO 13485 & ISO 17100 standards—provides comprehensive translation and localization solutions to help life science companies successfully manage global clinical trials, overcome regulatory hurdles and succeed in the global marketplace. Since 2000, Morningside has partnered with leading pharma, biotech, medical device companies and CROs to provide end-to-end language support for every phase of the product lifecycle—from pre-clinical to post-market. From translating PROs to localizing marketing materials for a global product launch, Morningside’s team of highly-skilled translators and project managers has the extensive life sciences expertise to get the job done—on-time and within budget.
Morningside’s extensive experience in life sciences has helped us develop certified processes and an extensive network of trained and qualified linguists for a wide range of life sciences projects–from global clinical trials to eLearning. Our team has in-depth industry knowledge of country-specific regulations, global markets, and the entire life sciences commercial supply chain.
Morningside’s life sciences translation services are provided by a leading team of certified and highly-trained medical linguists. Our scalable global network contains 1,500+ medical translators, proofreaders and Subject Matter Experts (SMEs) worldwide. We ensure that our translations are accurate, culturally adapted, and comply with all regulatory agency requirements. Our ISO-certified quality control process includes multiple rounds of editing and proofreading by medical translation specialists. Finally, our quotes are all-inclusive with upfront and transparent pricing. With more than fifteen years of life sciences translation experience, Morningside’s Life Sciences division can handle projects large or small on-time and on-budget.
Morningside’s QA processes are officially certified to the latest ISO 9001, ISO 13485 & ISO 17100 standards. The ISO 9001 standard applies to processes and procedures for maintaining a quality management system, and ISO 17100 defines the requirements for the processes, resources and other aspects for the delivery of quality translation services. The ISO 13485 standard applies to medical device companies and their suppliers. This certification is awarded to companies that have successfully implemented a quality management system that meets the medical device industry’s regulatory requirements, with a focus on risk management and strict quality control. Our QA processes are tracked and audited to ensure we maintain the highest level of medical translation quality.