Quality Commitment

Not all NAD+ is created equal

Some companies make their NAD+ using solvents to help the NAD+ dissolve and be administered, and some also use stabilizers to slow degradation and extend shelf life. At VAION, our scientists have developed a way to produce NAD+ and keep it in solution with zero solvents (other than isotonic water for injection) and zero stabilizers. The secret is in the process and conditions under which the NAD+ is made, not in adding ingredients that should not be there.

Because the NAD+ produced by VAION is just NAD+ in an isotonic solution, the side effects often associated with NAD+ administration are dramatically reduced, as many of these reactions are driven by solvents rather than the active ingredient. Without stabilizers, the NAD+ in our products is available in a much more active form too: This is why our customers report feeling NAD+ working even at very small doses of 50 mg.

Our NAD+ is available exclusively as NAD+ pens, NAD+ vials and NAD+ nasal sprays, giving you flexible options while maintaining the same uncompromising quality across all formats.

We are fully committed to giving you the absolute best NAD+ available.

A word from our Head of Quality and Regulatory Affairs

Our quality commitment to you

At our facility, we are committed to producing the highest quality NAD+ using a state‑of‑the‑art manufacturing processes. Production takes place in a rigorously validated cleanroom environment with double filtration air systems to ensure outstanding purity and cleanliness. We maintain complete traceability at every step and use only carefully qualified raw materials from certified suppliers.

To ensure sterility and safety, all materials used in our production are either sterile upon arrival or undergo validated sterilisation on site. During the filling of each pen, vial or nasal spray with NAD+, we work under advanced laminar flow hoods that maintain an essentially zero‑particle environment. Our NAD+ solution undergoes a dual 0.22 µm filtration process, providing highly effective removal of particulate and biological contaminants before final filling.

Each batch of NAD+ is released only after comprehensive quality control testing, including sterility and purity assessments, supported by independent laboratory analyses where appropriate. Our quality protocols are designed to detect and eliminate any deviations, and are embedded within a broader Quality Management System aligned with GMP and HACCP principles.

As Head of Quality Control and Regulatory Compliance, I oversee the entire process—from supplier qualification and raw material release through in‑process controls and final batch certification—to ensure that every NAD+ pen, vial and nasal spray meets our stringent internal standards as well as all applicable regulatory requirements.

In addition, we have implemented a robust quality control system to ensure the integrity and efficacy of our final product. Each batch of NAD+ undergoes comprehensive testing, including sterility, and purity assessments. The VAION quality control protocols are designed to detect and eliminate any deviations from our high standards, ensuring that every cartridge, vial or bottle delivered to our customers is of the utmost quality and reliability.

Our dedicated team conducts all activities under strict conditions, either fully gowned or within pharma-grade laminar flow hoods, ensuring the highest level of contamination control. The entire manufacturing process is designed and supervised by a Laboratory Lead with at least 15 years of hands-on experience in the medical device and pharmaceutical industries. Our Quality Controller has dual MSc degrees in Biotechnology and Quality Management and in Good Manufacturing Practice (GMP) manufacturing, ensuring that our NAD+ vials meet the most stringent VAION quality standards.