Summary — Quick Highlights
- ResolveMass Laboratories Inc. offers custom analytical method development quotes for HPLC and LC-MS tailored to your specific needs.
- Our scientific team brings decades of combined experience in pharmaceutical, biotech, and chemical industries.
- Fast turnaround times, validated precision, and regulatory-compliant reports.
- Specialization in complex APIs, impurity profiling, residual solvents, bioanalytical quantification, and nitrosamine analysis.
- Request your Analytical Method Development Quote today to ensure accurate, reliable, and reproducible results.
Introduction – Analytical Method Development Quote
When you request an Analytical Method Development Quote for HPLC or LC-MS testing, you’re not just asking for a price, you’re choosing a trusted lab partner who understands your sample type, your compliance needs, and your project deadlines. At ResolveMass Laboratories, we combine decades of industry experience with advanced instruments to design, test, and validate methods that meet global regulatory standards. From pharmaceuticals to medical devices, we deliver reliable results with clear documentation so you can move forward with confidence.
We believe that every testing project is unique, which is why our quotes are tailored to your exact requirements. By aligning our expertise with your goals, we ensure each method delivers accurate, reproducible results that are ready for regulatory review.
Learn more about our analytical method development services.
Why Our Analytical Method Development Quote Stands Out
At ResolveMass Laboratories, we design every method with precision, accuracy, and compliance in mind. Our scientists work closely with you to understand your specific project requirements, whether it’s for Extractables & Leachables (E&L), ISO 10993-18 compliance, or pharmaceutical impurity profiling. We use risk-based approaches to address potential interferences early, saving you time and preventing delays during regulatory submission. With our hands-on support, you can expect faster timelines without compromising quality.
Our commitment goes beyond delivering results, we aim to build long-term partnerships. By keeping communication open and transparent, we make sure you’re informed at every stage of the process, from initial design to final reporting.
Proven Expertise for Complex Projects
We have handled a wide range of samples across various materials, including plastics, elastomers, drug formulations, and medical device components. This experience allows us to predict and solve analytical challenges before they occur. Each method is custom-built to match your sample’s chemical and physical properties, ensuring it performs well in real-world use. Our process is detailed, controlled, and tailored to meet your project goals.
Get started today: Request a Custom Analytical Method Development Quote
Regulatory-Ready Documentation for Your Quote
When you receive an Analytical Method Development Quote from us, you also get the assurance that your results will be backed by documentation designed for immediate regulatory submission. Our reports meet the requirements of:
- FDA
- EMA
- ISO 10993-18
- USP <1663> and <1664>
We focus on clarity, traceability, and completeness so you can submit your results without additional formatting or rewriting.
Full-Service Method Development from Start to Finish
Our lab can manage every step of your method development — from initial planning to full validation and transfer. We also offer troubleshooting, re-validation, and training services for partner labs. By handling all stages in-house, we keep timelines short, results consistent, and communication simple.
This end-to-end approach means you don’t have to coordinate with multiple vendors or worry about gaps in project handover. From the first discussion to the final report, our team works seamlessly to ensure your method is reliable, compliant, and ready for real-world application.
Step-by-Step Process for Your Analytical Method Development Quote
| Step | Description | Outcome |
|---|---|---|
| 1 | Requirement Analysis | We discuss your project goals, regulatory needs, and sample matrix. |
| 2 | Method Design | Tailored HPLC / LC-MS workflow selection, column choice, and mobile phase optimization. |
| 3 | Feasibility Testing | Initial runs to verify sensitivity, selectivity, and robustness. |
| 4 | Optimization | Fine-tuning parameters to ensure accuracy and precision. |
| 5 | Validation | Full validation per ICH Q2(R1) and ISO 17025 standards. |
| 6 | Documentation & Reporting | Comprehensive final report, ready for regulatory submission. |
Start your journey with a custom method development quote
HPLC Method Development Specialties
Applications: We use HPLC to quantify active pharmaceutical ingredients (APIs), identify degradation products, and profile Extractables & Leachables (E&L) in a wide variety of samples. This technique is ideal for both routine quality control and complex analytical studies that require high accuracy.
Advantages: HPLC offers exceptional reproducibility and precise separation, even for complex mixtures containing multiple components. Its flexibility in column selection, mobile phase composition, and detection modes allows us to customize every method to match your specific needs.
Detection Modes: Our capabilities include UV-Vis, fluorescence, and refractive index (RI) detectors, enabling both targeted and broad-spectrum analysis.
Beyond these technical features, our team focuses on gradient optimization, stationary phase selection, and stability-indicating method development. We ensure that each method delivers consistent performance over time, supports regulatory submissions, and withstands the demands of long-term product stability testing.
LC-MS Method Development Specialties
Applications: LC-MS is our go-to technique for identifying unknown compounds, detecting trace-level impurities, and confirming molecular structures with high precision. It’s especially valuable in pharmaceutical research, E&L studies, and projects that require ultra-sensitive detection of complex analytes.
Advantages: This method offers exceptional sensitivity, allowing us to detect compounds at parts-per-billion or even lower. Its structural analysis capability means we can not only quantify a substance but also determine its molecular makeup, providing deeper insight into your sample composition.
Detection Modes: We employ a range of detection modes, including single quadrupole, triple quadrupole, and high-resolution mass spectrometry. This versatility lets us match the right setup to your project goals, ensuring optimal sensitivity, selectivity, and accuracy.
Our LC-MS workflows are designed for both routine monitoring and highly specialized investigative studies. By combining qualitative identification with precise quantitative measurement, we deliver data that is comprehensive, reproducible, and ready for regulatory review.
Commitment to Compliance and Quality
Every Analytical Method Development Quote comes with a guarantee of adherence to:
- ISO 17025 standards
- ICH Q2(R1) guidelines
- ALCOA+ data integrity
- FDA, EMA, and Health Canada requirements
We integrate compliance into daily operations, so your project remains audit-ready from start to finish.
How to Request Your Analytical Method Development Quote
When reaching out, share details such as sample type, target analytes, required detection limits, applicable regulations, and timeline. The more information we have, the faster and more accurate your quote will be. Contact us through our website, and our team will respond with a customized proposal.
You can get started immediately by visiting our
Contact page.
FAQs – Analytical Method Development Quote for HPLC / LC-MS
Your quote will outline the complete process — from method design and feasibility testing to optimization, validation, and reporting. We also include details on timelines, regulatory considerations, and deliverables so you know exactly what to expect before starting your project.
The development timeline typically ranges from 3 to 10 weeks, depending on the complexity of your samples, the validation requirements, and instrument availability. For urgent needs, we can discuss accelerated scheduling without compromising quality.
Absolutely. Our team is experienced in both Extractables & Leachables (E&L) analysis and pharmaceutical impurity profiling. We tailor each method to match your sample type, regulatory requirements, and detection needs.
We strictly follow ISO 17025, ICH Q2(R1), FDA, EMA, and Health Canada guidelines. Our processes are designed to meet audit-ready standards so your results are accepted by regulatory bodies worldwide.
Not always, the best choice depends on the target compounds, sensitivity requirements, and project goals. We evaluate your specific case and recommend the technique that offers the highest accuracy and efficiency.
Yes. We specialize in working with challenging or unusual sample types, from complex polymers to intricate biological materials. Our approach ensures accurate results even with difficult matrices.
Yes. We prepare complete data packages that are formatted for direct submission to regulatory agencies, saving you time during the approval process. These include raw data, validation records, and summary reports.
Conclusion
An Analytical Method Development Quote from ResolveMass Laboratories is more than a price sheet — it’s the start of a reliable, compliant, and scientifically robust process. With our deep experience, advanced tools, and commitment to quality, we help clients achieve faster approvals and lasting results. Partner with us today to take your HPLC or LC-MS method development to the next level.
Take the first step toward accurate, regulatory-ready results — Request Your Analytical Method Development Quote today or Contact Us for more information.
