Small Molecule LC-MS/MS Builds, From Tune To Matrix
- Protein precipitation, LLE or SPE chosen against recovery, cleanliness and runtime cost
- Column chemistry, gradient and MRM transitions tuned until the peak defends itself
A method is a chain of choices: extraction, separation, detection, and how the run proves itself. Development makes those choices deliberately and targets the criteria validation will grade against.
You can start from scratch, from our library of 500-plus prior methods, from a kit or from your incumbent's file. Reusing prior work saves weeks before validation begins.
No method exists anywhere: built from first principles around molecule and matrix
An in-house method adapted to your analyte, weeks saved before validation begins
A commercial kit qualified and hardened for your matrix instead of trusted blind
A working method transfers in with bridging, faster and cheaper than rebuilding
Method TransferA rescue: the failure diagnosed, the chemistry fixed, the history preserved
Method TransferEvery start ends at the same door: a development report written for validation
Method ValidationDevelopment drifts on undefined sensitivity targets and unlimited optimization. The SOW names the LLOQ, the matrix and the finish line.
500+Custom Methods Built Here Before Yours Ever Arrives
90%+Of Methods Developed Here Go On To Run Study Samples Here
Builds are quoted per method with the feasibility read priced separately, so you never commit a full budget before data exists. Typical small molecule builds complete in two to four weeks, ligand binding follows reagent timelines, and a senior scientist replies within two business days.
The quote you approve is the price you pay. Scope can only change through an SOW addendum you have already approved, which matters most on development work, where other labs treat every surprise as a change order.
One in three of the 100+ sponsors we work with every year is in at least a fourth consecutive year, and most of those relationships began with one method that worked.
NorthEast BioLab always exceeds expectations on bioanalytical assay development, validation, and sample analysis.
Our projects with NorthEast BioLab include successful method development, validation, stability studies during Clinical Phase I – IV studies.
We worked closely to implement the most efficient and cost-effective bioanalytical assay for our PK Studies.
NorthEast BioLab offers a science-based, hands-on approach to the latest bioanalytical platforms
We found their integrity as refreshing as readiness to provide creative scientific input and high-quality data
We trust NorthEast BioLab to design and execute streamlined, impactful bioanalytical projects
The build is the cheapest moment to get your program right, and the feasibility read means you never commit a full budget before data exists.
Bioanalysis is an essential tool in drug discovery and development for determining the concentration of drugs and their metabolites as well as various pharmacodynamics biomarkers in biological fluids….
From reference standard in hand to validation-ready, with every choice made in the open: extraction, transitions, gradient, acceptance targets.
Reference standard logged, stock plan set, internal standard chosen
Parent and product ions selected on the AB Sciex fleet, MRM pairs ranked
Protein precipitation, LLE and SPE compared on recovery and cleanliness
Column, gradient and runtime settled against peak shape and carryover
Multiple matrix lots screened, hemolyzed and lipemic where the study needs them
Development report out, validation plan drafted next door
Because development ends on purpose, at exit criteria we both signed, with validation already on the calendar.
Structure or sequence, matrix and required LLOQ are all it takes, and a feasibility assessment with a quote follows on the platforms linked below.
What sponsors ask when the study date is fixed and the method is not, answered.
A new method is the first step of a program, followed by validation and study samples on our instruments.