Pet Safety Standards for Compounded Veterinary Medications
At NPLabs Veterinary, the safety and well-being of your pets is our highest priority.
Discover our veterinary compounding services, find answers in our FAQ, or visit Pet Owner Resources.
Safety at Every Step
With over 19 years of experience in pharmaceutical compounding, NPLabs has established rigorous safety protocols that exceed industry standards. Our commitment to pet safety influences every aspect of our operation, from ingredient sourcing to final quality checks.
When your veterinarian prescribes a compounded medication from NPLabs, you can be confident that it has been prepared with the highest standards of safety, quality, and precision. Our dedicated team of pharmacists and technicians follow strict protocols to ensure that every medication is:
Precisely Formulated
Each medication is compounded according to exact specifications, with meticulous attention to dosage accuracy and ingredient compatibility.
Thoroughly Tested
Our quality control processes include multiple testing points to verify potency, purity, and stability of every compounded medication.
Sourced Responsibly
We use only pharmaceutical-grade ingredients from verified suppliers who meet our strict quality standards.
Carefully Documented
Complete documentation of every step in the compounding process ensures traceability and consistency.
Our Quality Assurance Process
Every medication that leaves our facility undergoes a comprehensive quality assurance process designed to ensure safety, efficacy, and compliance with the highest pharmaceutical standards.
Ingredient Verification
Before compounding begins, all ingredients are verified for identity, purity, and potency. We maintain certificates of analysis for all raw materials and perform additional testing when necessary.
Formula Review
Our pharmacists review each prescription to ensure the formulation is appropriate for the species, condition, and individual patient. This includes checking for potential drug interactions and contraindications.
Controlled Compounding Environment
Medications are prepared in specialized clean rooms with controlled temperature, humidity, and air quality. Our facilities exceed USP (United States Pharmacopeia) standards for compounding environments.
Multiple Verification Points
Throughout the compounding process, multiple pharmacists verify calculations, measurements, and procedures to prevent errors. Each step is documented and checked before proceeding to the next.
Final Quality Testing
Completed medications undergo final quality testing appropriate to the formulation type. This may include potency testing, pH testing, sterility testing, endotoxin testing, and visual inspection.
Pharmacist Approval
A licensed pharmacist performs a final review of the entire compounding record and physically inspects the medication before it is released for dispensing.
Regulatory Compliance & Certifications
NPLabs maintains strict compliance with all applicable regulations and industry standards to ensure the highest level of safety and quality.
EU GMP Compliance
Our facilities and processes comply with European Union Good Manufacturing Practice (GMP) guidelines, ensuring consistent production of high-quality medications.
ISO 9001:2015 Certification
Our quality management system is certified to ISO 9001:2015 standards, demonstrating our commitment to consistent quality and continuous improvement.
USP <795> & <797> Standards
We adhere to United States Pharmacopeia standards for non-sterile (<795>) and sterile (<797>) compounding, which define best practices for pharmaceutical compounding.
Regular Inspections
Our facilities undergo regular inspections by regulatory authorities and independent auditors to verify compliance with all applicable standards and regulations.
Partner with NPLabs for Your Pet's Medication Needs
Experience the difference that our commitment to safety and quality can make for your pets.