cGMP Manufacturing Services

Nitto Avecia Pharma Services' experienced staff is committed to first-time-right and on-time-in-full manufacturing support services customized to meet client needs. Nitto Avecia Pharma Services'  manufacturing personnel collaborate with the formulation, analytical and quality staff, to ensure an optimal transfer from a laboratory environment into a GMP manufacturing setting. Nitto Avecia Pharma Services'  state-of-the-art facility has been inspected by the FDA and is ISO 13485 certified.

Additionally, Nitto Avecia Pharma Services' parent company, Nitto Avecia, maintains a world-class reputation as a leader in oligonucleotide development and API production with over 20 years industry experience.