USP & FDA Standards & Requirements Services
At VaLogic, we leverage our extensive expertise in regulations and industry best practices to craft customized solutions that mitigate risks, elevate compliance, and guarantee the safety and quality of your products. Whether navigating the complexities of new drug development, upholding Good Manufacturing Practices (GMP), or gearing up for FDA inspections, you can count on us as your dedicated partner. We’ll ensure you achieve and sustain compliance at every turn, empowering you to focus on what you do best—delivering exceptional healthcare solutions.
USP-795
At VaLogic, we have the resources and experience to assist with meeting USP’s standards for compounding non-sterile drugs (including creams, lotions, capsules and pills), helping to ensure patient benefits and reduce risks.
USP-797
VaLogic can provide assistance in meeting USP’s standards for compounding sterile drugs (which are delivered through injection or intravenous infusion), helping to ensure patient benefits and reduce risks.
USP-800
In General Chapter <800>, USP outlines standards for the safe handling and compounding of hazardous drugs (such as those used in chemotherapy). VaLogic is sufficiently equipped to help individuals and organizations meet these standards.
503-A
VaLogic is adequately trained, licensed and certified to help pharmacies meet the FDA’s requirements to be designated 503-A compounding pharmacies. 503-A pharmacies are limited to compounding for individual use and do not work in large batches.
503-B
VaLogic is adequately trained, licensed and certified to help pharmacies meet the FDA’s requirements to be designated 503-B compounding pharmacies. 503-B pharmacies are allowed to compound in larger batches to save costs.
Have a question or need a quote? Give us a call!
Maryland Office
- Mon-Fri (8AM-5PM) EST
- 21 Byte Ct, Frederick, MD
- [email protected]
- (240) 529-1673
Texas Office
- Mon-Fri (7:30AM-4:30PM) CDT
- 1710 Preston Ave, Pasadena, TX
- [email protected]
- (713) 477-9247