QS Pharma will be at the 2009 AAPS Annual Meeting and Exposition
This year come visit Jack Milligan, our Sr. Director of Business Development and Bethanne Lee, our West Coast Business Development Manager at Booth 629. You can learn about our Contract Research and Analytical Services, Formulation Development, Manufacturing (Phase I-III), Preformulation, and Solid Dosage Processing.
We look forward to seeing you at AAPS in November!
For more information about our exhibit at AAPS or on your project, please call
at 610-485-4270 ext. 246 or
at 610-485-4270 xt. 265
October 2009 - QS Pharma Services Update
Expansion in Business Development from QS Pharma LLC! – Your leader in Contract Research/Product Development, Clinical and Commerical Manufacturing.
October 2009 - QS Pharma is pleased to announce the promotion of Bethanne Whalen Lee to the Business Development team at QS Pharma!
Bethanne will be based on the West Coast and will cover accounts and new business opportunities in that region. Bethanne has a BS in Medical Technology, MS in Biomedical Science and an MBA. She has been with QS Pharma for over 5 years initially as a chemist and promoted into the planning coordinator role. During that time she was responsible for analytical method development activities for client projects, writing and reviewing protocols, schedule planning, project management and proposal writing.
“Bethanne has demonstrated great acumen for business development and understands the importance of creating relationships with our customers. She will be a great asset for our existing and new customers on the West Coast” says Jack Milligan, Sr. Director of Business Development.
Dedicated to total customer support and scientific excellence, we offer enhanced development and manufacturing capabilities that broaden our Client-based profile through timely and superior quality services in the area of formulation development/clinical and commercial manufacturing.
Our mission is being the premier provider of CMC and current good manufacturing practices (cGMP) contract services from preclinical candidate screening through regulatory submission and commercial manufacturing to biopharmaceutical and pharmaceutical companies based on Quality with Speed®. We are dedicated to building long-term relationships with customers through quality and unparalleled pharmaceutical product development timelines and recognition as the leading pharmaceutical product development preferred provider.
For more information on your project, please call
at 610-485-4270 ext. 246 or
at 610-485-4270 xt. 265
August 2009 - Expansion Complete
QS Pharma completed a multi million dollar expansion project that focuses on our mission of being the premier provider of CMC and current good manufacturing practices (cGMP) contract services from preclinical candidate screening through regulatory submission and commercial manufacturing to biopharmaceutical and pharmaceutical companies.
April 2008 - Additional Capabilities in Formulation and Manufacturing
Within the newly expanded 6,000 sq ft of cGMP facilities, QS Pharma has added additional capacity by introducing 5 new manufacturing suites bringing the total development and manufacturing suites to 18.
March 2008 - Additional Capabilities in Analytical Research & Development
In addition to the increase in size of our laboratories, the Analytical Department has added more sq ft. for stability storage and testing to monitored manufactured supplies
