Business Details
38 Years
experience
Your Trusted Partner for Pharmaceutical CDMO Solutions
Pyramid Laboratories delivers comprehensive CDMO services for pharmaceutical and biotech industries, specializing in parenteral drug development and manufacturing. With 37 years of experience, our FDA-registered, GMP-compliant facility in Orange County, California, supports clients from pre-clinical stages through commercial supply. Our expertise spans formulation development, lyophilization, stability testing, and aseptic fill-finish manufacturing for vials, syringes, and cartridges. We prioritize quality, precision, and client partnership, offering tailored solutions for biologics, peptides, and small molecules.Our team of seasoned professionals ensures regulatory compliance and on-time delivery, with a proven track record of successful FDA inspections and global product distribution. We invest in state-of-the-art facilities and scalable capacity to meet evolving industry needs while maintaining the agility of a boutique CDMO. Our commitment to integrity and technical excellence has enabled clients to advance innovative therapies safely and efficiently.
Services
Drug Product Development
Lyophilization
Clinical Manufacturing
Commercial Manufacturing
Stability Studies
Method Validation
Aseptic Fill-Finish
Biologics Manufacturing
GMP Storage
Regulatory Support
Details
- Year established: 1988
Highlights and features
- We offer 37 years of specialized expertise in parenteral drug development and manufacturing.
- Our FDA-registered facility meets global GMP and ICH compliance standards.
- We provide end-to-end services from pre-clinical development to commercial supply.
- Our team includes experts with decades of experience in biologics and sterile manufacturing.
- We guarantee on-time, on-spec delivery with 100% testing accuracy.
Associations and certifications
- FDA Registered
- GMP Certified
- ICH Compliant
Services
Drug Product Development
We develop formulations for liquid and lyophilized parenteral drugs, optimizing stability and efficacy. Our process includes pre-formulation studies, analytical method development, and scalable manufacturing solutions. Clients benefit from tailored approaches for biologics, peptides, and small molecules.
Lyophilization
Our GMP lyophilization services ensure long-term stability for temperature-sensitive drugs. We provide process development, cycle optimization, and commercial-scale manufacturing. Clients receive validated methods meeting FDA and ICH standards for critical therapies.
Clinical Manufacturing
We produce GMP-compliant clinical trial materials with rapid turnaround. Services include vial/syringe filling, labeling, and global distribution. Clients gain streamlined processes for phases I-III with adherence to strict regulatory requirements.
Commercial Manufacturing
Our FDA-registered facility manufactures commercial drug products for international markets. We handle liquid and lyophilized formulations in vials, syringes, and cartridges. Clients receive consistent quality with scalable capacity and regulatory expertise.
Stability Studies
We conduct GMP stability testing including long-term, accelerated, and in-use studies. Our ICH-compliant storage facilities ensure accurate data for regulatory submissions. Clients receive comprehensive analysis to support shelf-life determination and product approval.
Questions
What services does Pyramid Pharma Services offer?
We provide drug development, lyophilization, clinical/commercial manufacturing, stability testing, and regulatory support for parenteral drugs.
Is Pyramid Pharma Services FDA-registered?
Yes, our facility is FDA-registered and complies with GMP and ICH standards.
Do you handle biologics manufacturing?
Yes, we specialize in biologics, peptides, and small molecule parenteral drugs.
Where is your facility located?
Our 90,000-square-foot facility is in Orange County, California, with global distribution capabilities.
How do you ensure product quality?
We maintain 100% testing accuracy, on-time delivery, and have passed 14+ FDA inspections.
Can you support international regulatory requirements?
Yes, our team provides expertise for global market compliance and product approvals.
