Medical and Regulatory Affairs
At ZeroRange Healthcare, our Medical & Regulatory Affairs teams possess a unique
combination of both scientific and management skills, with a focus on the
communications between internal and external stakeholders, returning insights and
generating values to contribute both scientifically and commercially, to the success
of a product development program in your organisation. Our offerings include:
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Medical Affairs:
Our Medical Affairs team engages expert clinicians and researchers, shares emerging science, and identifies trends in clinical practice. They excel in advisory consultation, capacity building/learning and development, medico-marketing, medical governance, and stakeholder engagement. We bridge the gap between commercial ambitions and medical ethics, providing balanced solutions that serve both patients' and business needs. - Regulatory Affairs: Our Regulatory Affairs team are experienced in all phases of development, including after drug approval and commercialisation. They ensure product compliance through meticulous registration, life cycle management, pharmacovigilance, adverse events reporting, and engagement with stakeholders. We navigate the complex regulatory landscape, ensuring smooth market entry and sustained success.
