Method Development and Validation
Whether you need expert testing consultation, method development or validation protocol design, Lancaster Laboratories offers you the widest range of laboratory techniques in the industry. We are also the only laboratory capable of providing method development for Comparator Product Testing. We support customers at various stages of the development/validation process and have a proven track record of success on full development and validation studies, optimization of existing research methods and transfer of previously validated methods.
Why Choose Lancaster Laboratories?
- We collaborate with you by thoroughly understanding your testing requirements, resulting in a method that meets your specifications, is validated for its intended use and is developed in the most efficient manner to maximize your research budget.
- We offer phase appropriate method validation, or when needed, we can perform your work under full cGMP compliance.
- We have the most experienced staff, performing more than 200 validation, verification and transfer protocols for our customers in 2011.
- We place an emphasis on building relationships and rapport with our clients. Thanks to our extraordinary rate of employee retention, you can be confident that you will have the same management team for the duration of your project, as well as for any future work you may do with us.
- For additional services you may need, our Method Development and Validation Team works hand-in-hand with our other departments to ensure a smooth transfer.
Leadership of Group:
Jon S. Kauffman, Ph.D. – DirectorOver 20 years with Lancaster Laboratories
Tom Lehman, Ph.D. – ManagerNearly 20 years with Lancaster Laboratories
Our technical writers have an average over 15 years industry experience.
Method Development & Validation for:
- Chemistry/Biochemistry
- Microbiology
- Bacteriostasis/Fungistasis for Sterility
- Inhibition/Enhancement Screening for Endotoxin
- AET and Microbial Limit
- Molecular and Cell Biology
- Cell-based assays
- ELISA
- qPCR
Protocol Writing for
- Method Validation
- Method Transfer
- Stability Protocol

Contact
Request additional information to start working with us today. Or call one of our Business Development Specialists at 717-656-2300.