Based upon the previous experience they bring to our facility both will play an immediate and critical role in client testing projects from day one
CLIFTON, N.J. (PRWEB)
June 14, 2023
CS Analytical Laboratory, the world’s only FDA regulated contract laboratory exclusively dedicated to providing regulatory solutions and qualification testing services specifically for drug product and medical device container systems, continues on its growth and expansion trajectory with the addition of two new laboratory analysts. We are pleased to announce the appointment of Nicolette Andrews and Alex Goldberg to the CS Analytical Team.
“We are excited to bring on two high quality Laboratory Team Members,” noted Brandon Zurawlow, Chief Scientific Officer. “Based upon the previous experience they bring to our facility both will play an immediate and critical role in client testing projects from day one.”
Nicolette, a trained biologist with prior cGMP laboratory experience will primarily work on USP 1207 CCIT programs to include Helium Leak Testing, Vacuum Decay, High Voltage and Laser-Based Headspace testing. Alex Goldberg, a Rutgers graduate with a Biomedical Engineering degree, will focus on the Routine Chemistry and Comprehensive and Complimentary Services side of the service area with a strong focus on package testing, Instron testing and a host of other ASTM, ISO and USP test method requirements.
CS Analytical has experienced substantial growth in all aspects of its operations over the past year. Executive Management has continued to implement programs and processes that ensure the growth and expansion program will always work to meet and exceed client expectations. Bringing on new team members that have the experience in critical test and service areas and the diligence and focus on client service are critical components to successful growth. The team is committed to working with all clients to ensure that the regulatory requirements for their container and package systems continue to meet the strict requirements set forth and expected by the FDA.
About CS Analytical Laboratory
The only FDA regulated, cGMP laboratory dedicated exclusively to the complex world of drug and medical device container and package qualification testing, the CS Analytical Team includes the world’s leading experts on all relevant USP and EP requirements and the thought leaders and pioneers on CCI (container closure integrity – CCI) testing. Offering a full suite of laboratory services to include all USP, EP and JP procedures specific to glass, plastic and elastomers as well as complete USP 1207 services that span basic feasibility studies, component qualification programs and advanced method development and validation for helium leak testing, vacuum decay, high voltage and headspace analysis leak testing. CS Analytical is the one source that can ensure your medical product container and package system meets the strict and complex regulatory requirements.
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