Good Manufacturing Practices (GMPs) represent the code of quality that LVT employs in all aspects of its operations. It includes
all aspects of pharmaceutical operations, including the production facility, analytical laboratory, employee training and other
critical elements. LVT uses an active systems approach to ensure that its products meet and exceed high quality standards.
LVT has a proven track record of GMP compliance. This is evident by the fact
that LVT has successfully passed numerous inspections by the Food and Drug
Administration (FDA). The results of these inspections have confirmed LVT's
commitment to upholding GMPs.
LVT’s facility resources include:
- Over 70,000 square feet of production space capacity, comprised of two facilities
- Wide range of expertise, covering many prescription product forms, including:
o Oral Solutions
o Tablets
o Capsules
o Liquid-filled capsules
o Suspensions
o Powders
