The 21st Century is the era of service, and our company is perfectly positioned to help you meet the growing needs of pharmaceutical, biotechnology, chemical, environmental and nutraceutical customers with compliance needs.
Satisfying customers across North America takes efficient, responsive professional method development and validation, including GC and HPLC method development and much more. Here's what we can offer you:
Welcome to the Future of Service!
  • Very experienced staff; rapid development at your site
  • Thorough documentation and data security
  • Confidentiality and Regulatory agency compliance
  • Confidence in final results
Key Performance Measurements
Our company is your #1 source for professional analytical development services. We evaluate performance by measuring achievement in 10 key areas:
1) Agreement on deliverables
2) Protocol development
3) Rapid optimization/development
4) Best laboratory practices
5) Method reliability
"We offer broad analytical chemistry method development / validation capabilities. We are not a typical contract laboratory. We provide analytical laboratory services and much more at your site. We're experts at providing well-thought-out solutions to challenging problems. Whether it's APIs, related substances, impurity isolation/ID, or sample preparation issues in varied matrices - we enjoy solving problems that will help get your products to market. Challenging solutions are performed rapidly, carefully, and completely that result in reproducible, validatable, transferable, and successful analytical chemistry methods."
                          
                                Gregory McLaughlin, CEO/Chief Analytical Development Scientist
6) QA/regulatory compliance
7) Final report documentation
8) Secure data/report storage
9) On-time delivery
10) Guaranteed customer
  satisfaction
New methods, redevelopment conforming to modern regulatory guidelines, optimization, characterization, release/stability methods, APIs/raw materials/drug products, sample preparation, rugged, reliable, rapid, and difficult projects.
FDA/ICH/EPA guidelines, specificity, identity, assay, impurities, linearity, range, accuracy, precision, repeatability, intermediate precision, reproducibility, DL, QL, system suitability, and robustness. Full and partial validation depending on stage readiness.
Method transfer, protocol development, deformulation, counterfeit product ID, sample prep, semipreparative impurity isolation, method development/instrumental consultation, HPLC/CE/validation/analytical techniques training.
Method Development
Method Validation
Other Services
WPBAD, 5093 El Claro E, West Palm Beach, Fl 33415          method.development@gmail.com      wpbad.biz
Call for a quote today! (561) 601-9730
Gregory McLaughlin - method Development
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