Board-Certified Clinical Cytogeneticist, versed in both the clinical and pharma environments on laboratory design, operations, testing and quality in the -omics world
Our Services
We offer quality audits of laboratories and processes. We can:
Set up and support quality monitoring and improvements in accordance with various regulatory agencies.
Perform gap analysis
Help with quality implementation and remediation.
Standard Operating Procedure writing and editing services are available in accordance with quality compliance guidelines. Edit a stock document for create bespoke documentation.
We have extensive experience with laboratory set up from design using lean six-sigma training for most efficient workflow to identifying and procuring laboratory equipment in both the clinical and pharmaceutical arenas. We offer:
IQ/OQ/PQ for equipment and process validation
Employee training and competencies.
Strategic planning and growth services
Laboratory staffing interviews and hiring to volume growth.
Physician education and consult on the implications of the testing and offer advice on the results.
Dr. Kaplan is board certified by the American Board of Medical Genetics- one of the disciplines within the American Board of Medical Specialties, with over 20 years of setting up and overseeing all aspects of laboratory operations. She is also qualified to report both cytogenetic and molecular testing clinical results.
Plan your next project or program with a clear path forward when it comes to safety testing and starting material viability. Discussing this early in program planning can save time and money on drug discovery R&D and manufacturing.
Ensure new test paradigms are a good fit for your clientele and future company goals. Train technical and sales staff on new testing and technical sales strategies
