Facilities & Equipment
QS Pharma is conveniently located about 15 minutes south of the Philadelphia International Airport and less than 3 miles from the main 95 North/ South Interstate.
The facility consist of over 43,000 sq ft of Analytical Laboratories and Drug Product Manufacturing space available which include cGMP suites and non-GMP development laboratories.
There are 14 manufacturing suites with dedicated Air and HVAC systems and the suites and equipment can accommodate batch sizes ranging from <1kg to over 500kg.
QS Pharma has state of the art Containment Manufacturing for handling High Potency, Cytotoxic Compounds, etc. QS Pharma’s containment classification is based on the industry standard PBLEC (Performance-Based Level of Exposure Classification) system. QS Pharma can handle a PBLEC Level 5 (or down 0.1ug/cu. meter) dependent on type of compound/dosage form and batch size. The four (4) Containment suites enable product development/ clinical and commercial manufacturing to take place in the facility.
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 based on Quality with Speed®. 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.
QS Pharma has and will continue to help build technologies to be the premier provider of CMC and cGMP contract services.