Regulatory and Quality Assurance Services

We specialize in Regulatory and Quality Assurance consulting and training for pharmaceutical, bio-technology and Medical Device companies on a global basis. NovaProbe Inc. has a group of highly skilled professionals capable of supporting a wide array of short and long term compliance acitivities including, but not limited to, GMP Training , GMP Audits, Gap Analysis, Vendor Audits, SOP Development, Part 11 Compliance Analysis, Corrective and Preventative Action (CAPA), Preparation of Common Technical Document (CTD), Mock FDA Audit, SOX Audits, Compliance per the Prescription Drug Marketing Act (PDMA) and Review of Validation Packages. In addition, we provide recommendations for remediating risks.