Overview: CER Writers needed for class I-III medical device products; primarily responsible for the preparation of regulatory documents and responses to regulatory authorities (with a focus on medical device products). Responsible for compliant writing of Clinical Evaluation Report (CER) additional document types included but not limited to: CEP, CMS-P, PMS-R, PSUR, PMCF-P, PMCF-R, SSCP-R Ensures the […]