Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs act...
Job Description: This position will play a critical role in ensuring the ethical and responsible conduct of clinical trials to protect study participants from potential harm, safeguard the integrity of the trial. By identifying potential p...
Responsibilities: Responsibilities include developing regulatory strategies, reviewing design input/output documentation, identification of applicable standards and guidance documents, performing regulatory assessments to determine the im...