YOUR TRUSTED PARTNER
INTEGRITY. EXPERTISE. RESULTS.
Rely on Avomeen's industry-leading experts to support any and all steps of the development pathway to bring therapeutics and devices to market. Leverage our decades of experience, unparalleled regulatory knowledge, and unwavering commitment to quality.
Avomeen stands with you each step of the way to ensure the integrity of results required throughout the regulatory process while providing the meticulous client service you deserve.
From concept to market and beyond, Avomeen's breadth of services can support every stage of the development life cycle.
Experience Avomeen's scientific depth and our team's consultative approach to customize our service offerings to fit your needs. No matter the scope of your project, Avomeen's experts are well-equipped to step in during any phase.
- Method Development & Validation
- Impurities, Unknown & Contaminant ID
- Proteomics & Protein Therapeutics
- Quality Control & Lot Release
- Stability Programs
- Elemental Impurities
- Cleaning & Process Validations
- Extractables & Leachables
- Packaging Compatability
- Regulatory Support
- GMP Small-Batch Manufacturing
- Preformulation Development
- Formulation Development
- Intellectual Property & Litigation Support
- Additional Support
READY TO PARTNER? SO ARE WE.
We're Not Just Any Lab. We're Your Lab.
Avomeen understands that you deserve more than just the one-size-fits-all protocols that other laboratories have to offer. Ensure compliance to regulatory standards while saving time and expense with our flexible solutions and modular approach.
Our team of Ph.D. scientists and regulatory experts take-on the burden of understanding regulatory standards and remaining current. Avomeen delivers so much more than trusted results. We deliver peace-of-mind.
We cover it all yet biopharma is our specialty.
We bring unmatched analytical expertise to solve difficult projects for which other labs are ill-equipped and won't touch.
Backed with a robust quality management system and built with compliance to the FDA and DEA.
Our internal processes are made to be flexible to fit most any client's requirements.
You'll get to know our experts as we communicate frequently from project initiation to completion and beyond.
Our wide-reaching capabilities incorporate industry-leading knowledge and expertise in the biopharma research, formulation, and regulatory processes. We've been helping to improve healthcare and speed time-to-market working with leading therapeutics and medical devices.
When routine testing laboratories don't have the experience or qualified experts to take on a project, they pass it on to the next laboratory. When those projects come to Avomeen, they get done.
That's because our unique blend of scientific, regulatory, and legal knowledge allows us to problem-solve from unusual angles. If it’s the right scope, we say yes when others say no to complex and challenging projects.
Every Avomeen project is backed by Ph.D. scientists who specialize in the regulatory knowledge and scientific applications specific to life sciences. When you put your project in the hands of our specialists, you can trust your results reflect the unparalleled knowledge of our industry-leading scientific minds.
We excel in building partnerships with our clients to ensure success in every stage of the development process from discovery to post-market, including lifecycle management.
Our dedication to our clients is apparent in everything we do. We work with you to tailor our processes to your program while maintaining scientific integrity and ensuring compliance to regulatory requirements.