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LaVaPharm LLC is an international GXP Quality Assurance (QA) Auditing and Consulting company established in 2013. We are a small woman-owned business entity with globally located full time and contract staff able to manage our client’s QA and Compliance Projects anywhere in the world.

Our expertise lies in Auditing and Regulatory Compliance Consulting in the fields of Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP), Good Laboratory Practices (GLP), and Computer System Validation (CSV).

The COVID pandemic has changed much in the world of business and clinical trials but the patient and volunteer still come first. We at LaVaPharm have been able to adapt quickly and have hands on experience in performing both on-site and remote audits running the gamut of the various types of audits in the GXPs. Like our customers we have adapted quickly to the uses of the ever evolving technologies, and have been successful in or ongoing audit and consulting conduct.

We ever remain agile and pragmatic able to provide and serve our clients with the best solutions and recommendations to ensure inspection ready trials and data.