With more than a decade of committed service to the peptide industry, CPC is a trusted provider of high-quality peptides to researchers and pharmaceutical companies all over the world. The CPC Group is comprised of peptide experts who have actively pursued peptide design and large scale manufacturing for more than 30 years, so your project is in good hands. CPC is the ideal peptide partner from concept to commercial for all of your cGMP needs.
Extensive knowledge developed through years of experience in the peptide industry is at your disposal.
SPPS, LPPS, ligation chemistry and fragment condensation methodologies
All protecting strategies (Boc, Fmoc, Cbz) can be used
Innovative purification and isolation techniques employed
Process development and scale-up competence insures a robust commercial process
Complex sequences and peptide modifications adapted to large-scale production
HIGH-CAPACITY cGMP FACILITY
CPC is expanding our manufacturing facility to better support your cGMP needs.
60,000 ft2 currently in operation
150,000 ft2 expansion in build out (Commission planned April 2015)
GMP batch sizes from gram scale to multi-kilogram scale
Qualified air and water systems
IQ, OQ, PQ qualified equipment
Class 100K, 10K, and 1K clean rooms
FULLY EQUIPPED LABORATORIES
CPC has an extensive portfolio of manufacturing equipment installed and qualified to produce cGMP-grade peptides in every stage.
Reactors with multiple volumes (20 - 2,000 L)
Hybrid synthesis reactor
Preparative HPLC systems with multiple flow rates
Chromatography columns with various inner diameters (up to 18 in)
Fast protein liquid chromatography (FPLC) systems
Blenders and evaporators
A dedicated Quality department verifies full cGMP compliance throughout production, as well as testing and documentation standards in accordance with the most stringent FDA requirements.
In-process, release and environmental control testing performed
Standard release testing performed in-house
Audited contract laboratories available for additional testing
Method development and validation, formal method transfer
Stability studies (ICH) and forced degradation
Process development support (peak homogeneity, impurity characterization)
A typical cGMP peptide is tested at CPC using the following methods:
Purity (HPLC, UPLC)
Molecular weight (MS)
Moisture content (Karl Fisher
Additionally, our QC department is fully equipped and additional analysis can be performed upon request.
CPC provides complete support for your IND and NDA filings in the USA as well as all international filings and all required regulatory support for your peptide APIs.
Batch record review
Document management and control
CAPA follow up and tracking
Phase appropriate control systems consulting
DMF compilation and submission
Annual product reviews
GENERIC PEPTIDE APIs AVAILABLE OR IN DEVELOPMENT
We will work closely with you throughout the project and adopt any previous chemistries that can shorten your clinical trials and reduce the risks in clinical filing complications.
Liaison to CPC operation
Cross-functional links from CPC operation to customer operation
Project history documentation
The satisfaction of our customers is the most important reason for our continued growth and success. One critical ingredient is maintaining the confidentiality of trade secrets and proprietary information released to us by our customers. CPC will assure the complete confidentiality of all proprietary information we receive during the course of fulfilling any of our custom services.
COMPLETE PRODUCT LIFECYCLE SUPPORT
CPC provides comprehensive product lifecycle support at every phase.