preferably in human medicines, including complementary medicines and medical devices for end-to-end regulatory
submission of new products, with a focus on complementary
preferably in human medicines, including complementary medicines and medical devices for end-to-end reg
submission of new products, with a focus on complementary
preferably in human medicines, including complementary medicines and medical devices for end-to-end regulatory submission of new products, with a focus on complementary medicines and medical devices.
validation and calibration activities for a GMP complementary medicine and cosmetic manufacturing facility. Develop