Our Capabilities: Unlocking Potential
At Cellipont Bioservices, we’re dedicated to empowering our clients to bring life-changing medicines to patients worldwide. With our best-in-class cell therapy development, analytical, and manufacturing capabilities, we’re your trusted partner in turning innovative ideas into impactful realities.
Why Partner with Us for Manufacturing?
- cGMP Manufacturing: Ensuring the highest standards of quality and compliance in every step of the manufacturing process
- Analytical Method Development: Crafting robust analytical methods to ensure the safety, potency, and purity of your therapies
- Process Development: Optimizing processes for efficiency and scalability, from research to commercialization
- GMP Quality Control Lab: Rigorous quality control to guarantee the integrity and consistency of your products
- Method & Process Validation: Thorough validation procedures to meet regulatory requirements and ensure reliability
- Documentation and Batch Record Development: Comprehensive documentation and batch records tailored to your specific needs
- cGMP Stability: Conducting stability studies to assess product shelf life and maintain quality over time
- Regulatory Support: Navigating regulatory hurdles with confidence, from filings to inspections
- Sterile Fill/Finish: Ensuring the sterility and integrity of your products through precise fill/finish processes
- Program Management: Seamlessly coordinating every aspect of your project for timely and successful outcomes
Contact us at [email protected] for more info on our manufacturing services.