Frequently-asked questions
Are you a global business?
Yes, we are a global organization fully licensed in: US, EU, UK, and China. We also have global sourcing capabilities in: North America, Europe, Middle East, Africa, APAC, and LATAM.
We have also served 50+ countries around the world for clinical trial supply.
We have also served 50+ countries around the world for clinical trial supply.
Can you obtain documentation?
Yes, we are able to access documentation such as: CoA, CoC, CoO, BSE/TSE statements, MSDS, Stability Data, Statement of Equivalence, etc.
We will review your study requirements on a case-by-case basis and assess the market to identify what is accessible and what is required in order to access your required documents.
We will review your study requirements on a case-by-case basis and assess the market to identify what is accessible and what is required in order to access your required documents.
Can you support large Phase III global studies?
Yes, we have extensive experience providing support to Phase II & III studies around the world. Our clients lean on our industry expertise. We provide comprehensive sourcing strategies to help you to make informed decisions that will assist in mitigating risk in your supply chain, managing costs and managing waste.
This allows you to reinvest time and money back into your R&D for the long-term.
This allows you to reinvest time and money back into your R&D for the long-term.
>>> Our people
Our company is our people, and our people are on hand to speak directly with you
Mark Johnson
Technical Director, Strategic Partnerships
