LaVaPharm Consulting was established as an Independent International GxP Auditing and QA Consultancy firm in June 2013 headquartered in Temecula, California with an affiliated office in Southern Europe.
With over 50 affiliated Quality Expert Consultants located globally (including South America, Africa, Asia and the Pacific Rim) we can accommodate any need at any time.
LaVaPharm can provide you the global knowledge and reach that is needed in today’s international marketplace including audits of multicenter clinical trials, pharmacovigilance affiliates and various third party vendors. While cutting travel costs when possible.
We provide you a choice of consultant’s to meet your needs, whether short term, long term, or even on-site at your location.
We take a pragmatic view and have worked with companies of all sizes. Whether large, medium or micro pharma is irrelevant to compliance, but what works for one does not work for all, so we analyze your situation and offer the best fit for each client’s expectations.