Working in medical & pharma, and being responsible for people’s health and lives, make for a highly sobering experience. Great responsibility comes with rigorous standards and strict regulatory laws, for both your work and that delivered by service providers.
SWS stands by you with an in-house physicist and medical practitioner, and multiple expert medical translators. We deploy industry-standard glossaries, professional project managers and several layers of quality control, in order to make sure we comply with your most rigorous standards.
Most frequent document types:
– Research and development
– Clinical studies
– Post-marketing surveillance of medicinal products
– Regulatory laws for marketing medicinal products
– Pharmaceutical marketing
– Summary of product characteristics (SmPC)
– Patient-reported outcomes (PROs)
– Case report forms (CRFs)
– Medical records