VPCI has proven its success through an excellent FDA approval record
VPCI has been supporting the Pharmaceutical Industry with a growing portfolio of services since 1978. We are based in the United States, providing a virtual bridge of services that connect Pharmaceutical companies throughout Europe to the regulatory environment of the FDA. Our clients include API manufacturers, a wide variety of finished dosage form manufacturers, CMOs, intermediate processors, testing facilities, medical device manufacturers, homeopathic and food ingredient suppliers.
To provide the necessary depth and quality of our services, VPCI collaborates with a global base of associated consultants. We can staff our projects with a combination of U.S.-based experts and European-based technicians to allow our clients the benefits of a cost-effective engagement, along with the best and most qualified consultants available for the particular task at hand. We have the ability to communicate with clients and regulatory agencies in a number of languages.
VPCI personnel have participated in the design, writing and implementation of a variety of pharmaceutical regulations. We have also assisted regulatory agencies worldwide (U.S.A., Italy, Mexico, Brazil, Japan) in training for their internal inspectors. Several industry standards, books and guidelines have been co-authored by VPCI personnel including those published by the PDA (Parenteral Drug Association), IEST (Institute of Environmental Science and Technology), and ISPE (International Society for Pharmaceutical Engineering).
We have earned a well-deserved reputation of trust, expertise, and highly successful project outcomes. We believe that expertise from our many years of experience and hard work equals positive results.