What We Do
As your trusted drug product CDMO, we offer one point of access for the broad pipeline of services supporting every stage of the parenteral product lifecycle, from preclinical development to commercial scale. Whether you come to us for our analytic and microbiology capabilities, stability testing and validation, or aseptic fill-finish manufacturing and lyophilization services, you’ll find our tailored support and attention to quality at every touchpoint.
Our expertise
Experience and Excellence: Our Four Pillars
Every service we deliver is designed to harness our technical excellence, breadth of experience and continual innovation to bring your drug to patients—with safety and quality assured.
Client focus and dedication
Expertise and know-how
State-of-the-art facilities
Scalable capacity
Our services
Any Molecule, Every Stage. Services Designed for You.
Whether you have a drug idea or a proven innovation, our full suite of services will move your program forward to your next drug product development or GMP manufacturing milestone.
Drug Product Development
Formulation & process development for liquid & lyophilized products
Lyophilization
Development and GMP manufacturing for lyophilized drug products
Clinical Manufacturing
GMP manufacturing & distribution for clinical trials
Commercial Manufacturing
GMP Drug Product Manufacturing for International Markets
Biologics & Novel Modalities
Drug product development & manufacturing for biologics and other novel modalities
Analytical Services & QC Testing
Method development, validation and testing
Stability Studies
Short-term & long-term stability studies at all ICH conditions
Quality Assurance & Regulatory Support
Our dedicated Quality Assurance team ensures that all work is conducted in strict compliance
Labeling, Storage & Distribution
ICH-compliant GMP storage. Global distribution
How we help
Integrated Programs at Every Stage
Our turnkey solutions can be customized as needed to create a program that addresses your specific requirements, across the drug development lifecycle. Whether you’re in the preclinical phase or need large-scale commercial manufacturing, we can help you accelerate progress and meet your development milestones, faster.
Contact us
How Can We Help?
Let us apply our 37+ years of experience as a fill finish CDMO to help you solve your drug product development and supply challenges. Learn more about what it means to differentiate your development process and GMP manufacturing with Pyramid Pharma Services.