As pharmaceutical and medical device companies expand distribution of medicines and products around the globe, compliance to timelines is critical to avoiding delays or losing a spot in the release cycle.
In the pharma and medical device industries, providing quality, on-time submissions to local regulatory bodies is probably the single most important part of your business. Navigating the labyrinth of country-specific regulatory submissions can take weeks or even months.
At Lionbridge Life Sciences, we can help you provide on-time quality submissions to local regulatory bodies—every time. Our dedicated project management and language supply chain teams focus on two things for both pharma and medical device clients: Readiness and delivery.
Our Global Regulatory Solutions rely on a network of extremely qualified medical resources, each with years of direct experience working with local Health Authorities around the world (the European Medicines Agency [EMA], China’s SFDA, Japan’s PMDA, and South Korea’s KFDA, to name a few).
We adhere to validated certifications and rigorous methodologies to deliver high-quality regulatory translation services and strategy, while focusing on fast turnaround times to help you comply with the ever-changing, ever-challenging global regulatory environment.
You can also take advantage of technology as a managed service, an easy-to-implement, flexible solution for multilingual asset management (translation memories, glossaries, style guides), streamlined in-country language review processes and integration with labeling, and other Content Management Solutions and authoring tools.
Lionbridge Life Sciences is ready for you in every way—ready to deploy fully integrated solutions with a proven, rigorous process. Ready to scale globally and deliver locally. Ready to provide the multilingual regulatory and subject matter expertise you need to stay ahead.