Expertise at every step
State-of-the-art technology
Cutting-edge science
End-to-end services
Expertise at
every step
State-of-the-art technology
Cutting-edge science
End-to-end services
Fully integrated drug development, testing & manufacturing
We are a US-based, world-class CDMO driven by the belief that scientific expertise and manufacturing excellence combined can bring life-altering therapies to patients faster. Our team of industry-leading experts supports a diverse range of projects with broad experience and constant innovation. Our comprehensive portfolio of capabilities from lab-scale development through commercial manufacturing ensures quality, scalability, and speed for cutting-edge therapeutics from a single source at every stage.
Advanced technology, collaborative approach
We have invested in state-of-the-art facilities and equipment to ensure delivery of the highest quality sterile injectable products. Our team focuses on building collaborative relationships with our clients, while leveraging our subject matter expertise to deliver a seamless experience from process development through distribution.
Link to: Product Development – new
Product Development
On-site development and testing laboratories led by highly experienced scientists
- Process development and optimization
- DoE and QbD study design, execution, and statistical analysis
- Technology transfer and scale-up
Link to: Analytical Services – new
Analytical Services
Advanced characterization and leading-edge technology
- Analytical method development and validation
- Full raw material release and USP <1> injectable testing for finished goods
- Stability testing across all ICH Zones for impermeable and semi-permeable containers
- Testing for residual solvents, elemental impurities, extractables & leachables, photostability, nitrosamines, container closure integrity, and thermal cycling
Link to: Manufacturing Services – new
Manufacturing Services
Advanced sterile filling systems to support diverse container types and batch sizes
- Formulation scale of 1 L to 4000 L using stainless steel and single-use technology
- Fully isolated filling lines for vials, syringes, and IV bags, including drug-device combination products
- Automated visual inspection, assembly, labeling, packaging, and serialization
Build your career where innovation meets impact
Join our team and contribute toward providing high quality pharmaceutical development and manufacturing solutions to our clients.
With state-of-the-art facilities and equipment, and a team of technical experts, we are focused on making a difference for our clients and the patients who benefit from the novel therapeutics we deliver.
If you thrive in a fast-paced, growth-driven environment where your contributions can make a direct impact, we would love to hear from you.
Connect with our experts
Meet us at an upcoming event
BIO International
Boston, MA | June 16-19, 2025
Contract Pharma
New Brunswick, NJ | September 18-19, 2025
CPHI Worldwide
Frankfurt, Germany | October 28-30, 2025
DCAT
New York City, NY | March 23- 26, 2026
CPHI NA
Philadelphia, PA | June 2-4, 2026
BIO
San Diego, CA | June 22-25, 2026
News at August Bioservices
Parenteral Perspectives
Exploring innovations, challenges, and future horizons in parenteral drug delivery.
CDMOs: Key Leader Insights
For this roundtable, Contract Pharma called upon thought leaders across the pharmaceutical services sector to address “3 Key Trends” impacting the CDMO industry in 2025 and beyond.
Development to Delivery: A CDMO’s Guide to Strategic Scale-Up
Bringing a sterile injectable product from development to commercialization requires a seamless scale-up process—one that minimizes risk, optimizes efficiency, and ensures regulatory success. In this exclusive webinar, experts from August Bioservices will discuss the critical factors that make or break a successful scale-up, sharing insights from a CDMO’s unique perspective.