16 years of experience as Quality Assurance Responsible Person, Qualified Person Responsible for Pharmacovigilance/Local Safety Responsible
6 years of experience as a Consultant for Quality Management Systems (QMS), Business Development focusing on Quality and Regulatory Affairs (RA), and Quality Pharmacovigilance
Specializes in creating QMS documentation compliant not only with Good Manufacturing Practice (GMP) and Good Storage and Distribution Practice (GSDP) requirements, but also with Good Pharmacovigilance Practices (GVP) to meet Quality PV standards
Holds a Diploma in Pharmacovigilance Auditing/Lead Auditor from UK
Holds a Diploma in Pharmaceutical QMS Auditing/Lead Auditor from UK
Certified GSDP Pharmaceutical Quality System Auditor and Quality Pharmacovigilance Auditor
Qualified International Trainer accredited by the International College in London
Owner and Founder of the State Of Practices Consultancy Center (SOP Center)
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