With years of experience servicing some of the world’s largest pharmaceutical and medical device companies, SH3 has a proven quality process driven by your industry standards. We understand that your industry is highly regulated. That’s why we focus on complete quality management, measurability and traceability. SH3 is equipped to help you scale your growing business. We have ISO 9001:2008, EN 15038:2006, EN ISO 13485:2012 certifications and are J2450 compliant.
SH3 builds partnerships with our clients to meet your goals whether those are cost savings or reduced time to market. SH3 is a trusted name for quality translations in the life science industry.
Working with leading healthcare companies, we use only translators that have the expertise and education required to provide quality translations. Pharmaceutical organizations that have recently expanded or are in the process of expanding their global reach quite often face complications in foreign markets. That is why it is important that your translation partner has the knowledge and expertise to help your content meet international protocols and regulations.
With global clinical trials, accurate translation is one of the most important aspects of your pharmaceutical process. At SH3, our dedicated experts drive the proven process surrounding the centralized management of clinical trial localization. During this process we can help ensure that your business meets set regulatory deadlines.
Medical Device and Biotech
The medical device and biotech industry is driven by strict regulations that demand quality, and this can grow more complicated once you plan on lauching your products globally. SH3 is equipped to help you navigate through this process while ensuring that your content meets international standards and regulations. SH3 can offer expert assistance in creating the right approach for your globalization efforts.
SH3 has the capacity to meet and exceed your deadlines, complex requirements and regulatory compliance.