Clinical Supply Chain
We focus on quality and speed to ensure your clinical studies are completed on time and within budget.
Clinical Supply Chain
Vici can help with all your clinical supply chain needs for non-sterile products as your one-stop R&D partner. This includes oral, buccal, topical, and suppository products. We can manufacture Phase I/Phase II clinical trial materials in-house and Phase III and commercial materials at our sister manufacturing company, also conveniently located in Maryland USA.
We offer the following services to help you quickly get from concept to clinic:
- Clinical supply chain management
- Phase I clinical supplies manufacturing
- Phase II clinical supplies manufacturing
- Phase III clinical supplies manufacturing
- Placebo formulation development and manufacturing
- Clinical packaging, including blinded clinical packaging
- Release testing and generating COAs for clinical study materials
- Accelerated and real-time stability studies to support IND filing and clinical study shelf-life dating
- Clinical supply material (or investigational product) CMC investigations if necessary
- Export of clinical supply material to foreign countries (such as Europe, Australia, or India)
- Pilot or pivotal bioequivalence clinical supplies manufacturing for generic (ANDA filing)
We are flexible and innovative. Contact us to see how we can help you with your clinical trial needs.
We are licensed for DEA manufacturing (Schedule I-V) and testing Phase I/Phase II clinical trial supplies. We are also DEA-licensed for the manufacturing and testing of Schedule II-V materials for Phase III clinical trials.
Clinical Supply Management & Manufacturing
Our clinical supply chain capabilities include:
