GMP Engineering for the Biopharmaceutical Industry
ABOUT STOLLEY ENGINEERING
Who we are
About Us
Stolley Engineering is a globally operating company with expertise in GMP.
We specialize in validation and qualification of sterile manufactured biopharmaceuticals, biosimilars and gene therapies. To date, we have helped clients sail their products through regulatory scrutiny and reach manufacturing authorization.
We hold 20+ years of proven and sound knowledge in Bioengineering, Cell and Molecular Biology, and GMP Engineering.
Project lead or team work will be provided by our well-versed and long-term experienced engineers. We perform on-site training and give presentations. Our services are tailored to products, processes and customer needs.
Our aim is to support and contribute to the implementation of GMP quality standards as they pertain to the Biopharmaceutical Industries.
Together we are driving GMP.
Sincerely, yours Sabine Stolley
References will be available upon request. | Please use our contact form!
Our Mission
Stolley Engineering is leveraging their expertise to solve GMP needs between customers and regulatory authorities.
Our Vision
With enthusiasm and passion for medical innovations and technologies, we guide our clients through validation and qualification operations, on their road to cGMP compliant processes.
What We Stand For
Expertise and experience, commitment and dedication, mind and reason – this is what makes us uniquely different.
Customers We Serve
- Biopharmaceutical Industry
- Biotech Companies
- CDMOs
- Treatment Centers for Gene Therapies
- Healthcare Sector
Languages We Speak
- English
- German