At CMC, we work closely with select partners to integrate them into project teams.
Guiding principles:
- Cooperative team relationship with the development partner
- Commitment to quality
- Dedication to meeting partner's goals through the on-time delivery of product and information
At the end of the project, our partners get more than drug substance and the associated documentation: You and your product will benefit from our years of experience in process development and cGMP clinical manufacturing.
When you initiate work with CMC, an experienced project manager will be assigned to your project. This manager will work with you to:
- Ensure efficient communication
- Track tasks to focus on key objectives
- Make certain your needs are met as situations unfold or change
Before a project commences, we work with you to establish several important documents outlining exactly what work will be done and what products and reports you will receive. These jointly developed documents ensure that the services provided will be completed in a timely manner under the highest quality standards.
A typical agreement includes the following documents:
- Scope of Services
- Timeline
- Manufacturing Agreement
- Quality Agreement
- Materials to be transferred
- Product Specifications
- Pricing terms