Safe Harbor Pharmacovigilance, LLC provides client-focused clinical trial safety services and management to pharma and biotech companies. The company delivers high quality services in safety management, medical monitoring, Safety Review Committee (SRC) and Data Safety Monitoring Board (DSMB) services. Safe Harbor Pharmacovigilance, LLC utilizes experienced and professional staff to provide efficient, timely and accurate deliverables; services include clinical trial medical monitoring and consulting, serious adverse event management, regulatory safety reporting, individual case report and aggregate safety reviews, coding entry and coding reviews, and DSMB coordination and management. Safe Harbor Pharmacovigilance, LLC provides top quality, flexible and cost-efficient solutions for today’s clinical research outsourcing needs.
The client is our focus: we ensure that the client's needs are met and that the safety component of a clinical trial is performed in the highest quality manner possible. Ultimately, our goal aligns with the client’s goal – successful completion of a clinical trial with accurate and thorough data collection, enabling product development and approval and new drugs brought to patients in need.
Our expertise and commitment to pharmacovigilance allows our clients to focus on the core business of running a clinical trial while we ensure that pharmacovigilance information is properly collected and regulatory requirements are met. We will be your Safe Harbor.
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