Your CDMO Partner
from Concept to Clinic

Delivering drug development solutions for emerging pharma.

CDMO SERVICES

Formulation Development

Unmatched formulation development expertise to accelerate your drug development program.

Analytical Testing

Providing you with testing data you can rely upon.

Clinical Supply Chain

We focus on quality and speed to ensure your clinical studies are completed on time.

Regulatory Services

Providing you with 505(b)(2) and ANDA regulatory strategy and filing services.

R&D Consulting

We provide a range of services to address all your R&D needs.

What We Do

We are experts at formulation development, analytical method development, manufacturing process development and tech transfer, CRO management for BE studies, CMC regulatory documentation, and regulatory filings.

About

Vici Health Sciences

Vici delivers end-to-end drug development solutions for small pharma. We provide formulation development, analytical method validation and testing, cGMP clinical supplies manufacturing, FDA regulatory services, and CMC R&D consulting services. We are experts in NCE molecule development, NDA 505(b)(2), and ANDA development programs. Our experienced formulation scientists and chemists solve problems through innovation, speed, and flexibility offering excellent value for companies needing better R&D outcomes. Vici operates a pharmaceutical R&D center of excellence in Maryland, USA.

Latest Updates

505(b)(1) vs 505(b)(2): Understanding the Key Differences in FDA Drug Approval Processes

505(b)(1) vs 505(b)(2): Understanding…

The 505(b)(1) pathway is typically used for new…

Patient Compliance Through Drug Delivery Systems

Patient Compliance Through Drug…

Lack of patient compliance in medication is a…

What is CMC?

What is CMC?

In the pharmaceutical industry, CMC stands for Chemistry…

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