LaVaPharm Consulting is an international service provider of expert Quality Assurance GxP Auditing, Consulting and provision of Regulatory Training for the Pharmaceutical, Biotechnology and Device healthcare industries. With a large global network of expert GCP, GLP, CSV and GVP consultants LaVaPharm is able to meet the client's needs of auditing multicenter, mutli-vendor faceted clinical trials while managing to keep travel costs down. Our team has been in the client's shoes and can advise on any and every aspect of preparation for regulatory inspection. We currently have consultants located in the US, Canada, South America, Europe, Russia, South Africa, the Middle East, and Asia Pacific.