APCER Pharma provides comprehensive drug safety, regulatory services and risk management programs to pharmaceutical, biotechnology, medical device, and consumer products companies. APCER continues to deliver on-time services to its customers in the US, Europe and Asia and it is emerging as the leader in offering ‘right sized’, fully integrated and serviced solutions to the Industry.

Customers benefit from leveraging our investments, experience and training at a fraction of the cost of their existing or planned operations in Pharmacovigilance and Regulatory areas. We are confident about meeting the compliance needs of our customers and offer our customers service level guarantees and objective ways of measuring our performance.

Our processes have been successfully inspected by regulators several times, we take pride in providing solutions that are compliant and we provide the following capabilities to our clients:-

• Risk Evaluation, Signal Detection & Aggregate Reporting
• Clinical Safety Monitoring & Reconciliation
• Post Marketed Products Pharmacovigilance
• Medical Science Liaison and Medical Affairs Services
• Device Safety Monitoring, Product Complaint Handling
• Regulatory Operations Services
• Hosted Safety Database & Regulatory Submission – Secure, 24x7 Supported

Our experts provide services to pharmaceutical companies, biotechnology, biopharmaceuticals, device and diagnostics companies. For many of our clients we represent them as their ‘Responsible Person’ or ‘Qualified Person for Pharmacovigilance (QP-PV)”, responding and reporting directly to regulators on behalf of our clients.

Reach out to one of our team members and we will immediately respond to your needs with well thought through solutions. Within North America, please call us at (877) APCER NA and in Europe, call our London office at +44 208 326 3220.