Drug discovery > Clinical Development Products & Reviews

An entry-level online QC data management software providing basic QC rules, charts, and peer reports  

An entry-level desktop QC data management software providing basic QC rules, charts, and peer reports  

Advanced online QC data management software to facilitate regulatory compliance under CLIA and ISO 15189 and provides advanced charts, reports, data analysis, and comprehensive audit trails.  

Advanced desktop QC data management software for expert users to facilitate regulatory compliance under CLIA and ISO 15189 and provides advanced charts, reports, data analysis, and comprehensive audit trails.  

The complete leak proof and gas permeable packaging solution for culturing and shipping in 24/96/384 multiwell plate formats.

Leak proof and gas permeable secondary packaging material available in two sizes to combine with your own cell culture vessels.

The Wieslab® Complement Pathway-specific Functional assays are well known within the complement world, used both as an alternative to hemolytic assays and a diagnostic tool for complement functional assessment. Based on the ELISA setup, the assays provide a robust and standardized assay platform, delivering fast, reliable, and easy-to-interpret results within 3 hours.

The high speed Micronic Rack Reader DT520 is designed to quickly read single tubes and rack barcodes in one ergonomic device. Readout time is less than one second.

The Cipher dissolution control software is a Windows-based application designed and developed by Distek which can be installed locally or networked providing full access to any Distek dissolution instrument on the network. Cipher offers the flexibility to set the level of security appropriate for your laboratory and will meet 21 CFR part 11 compliance.   

Recombinant PURedit Cas9 protein from Streptococcus pyogenes is a ready-to-use reagent for genome engineering experiments

Enable assessment of drug transport by comparison between the wild-type (WT) and knockout cell lines

Megarobo's new MRA-LSF-840 series ultra-high-throughput kit assembly system can meet the needs of reagent card assembly in terms of throughput, compatibility, and yield. At the same time, it is equipped with card loading and packaging modules, and each module can be operated independently or combined for production.  

Efficient: Up to 8000-10000 pcs/h Flexible: Compatible with multiple types of tubes such as disposable virus sampling tubes Intuitive: Visualization software & touch screen Modular: Including laminar flow, labeling and coding, and CCD modules, allows for personalization Stable: Stable operation, high yield rate Effortless: Only 1 -2 people are needed to complete the whole process

Efficient: Up to 8000-10000 pcs/h Flexible: Compatible with multiple types of tubes such as disposable virus sampling tubes Intuitive: Visualization software & touch screen Modular: Including laminar flow, labeling and coding, and CCD modules, allows for personalization Stable: Stable operation, high yield rate Effortless: Only 1 -2 people are needed to complete the whole process

The Micronic 1.40ml internally threaded screw cap tubes are available with a V- or U-shaped interior bottom.

Learn how to perform a gap analysis of laboratory quality activities to help your laboratory meet minimum QMS requirements.

QPS Global Custom-Built Regulatory Services Can Transform Clinical Trials.  QPS Global Regulatory Affairs (GRA) service offerings focus on helping pharmaceutical, biotechnology, and medical device companies to develop custom-built research solutions that forge expedited regulatory pathways from discovery to global commercialization and onwards through product lifecycle support. 

Moving quickly and safely through Phase I/IIa trials is critical to successful drug development.  The QPS Phase I research facilities feature more than 550 beds across six strategically located facilities on three continents. QPS is well known for its success in first-in-human clinical trials. All Phase I sites are staffed by expert clinical pharmacology teams that routinely conduct hundreds of phase I/IIa studies annually. 

At QPS, we realize that in today’s late stage drug development space you face many challenges.  With our deep experience and broad global presence, QPS is in an excellent position to offer solutions to all of the above needs. With its site management & monitoring teams operating from 30 locations on three continents (Asia/Pacific, USA, and Europe), QPS has become a new strong player in Phase II/IV clinical research services. 

Automated microbiology specimen processing instrument.

Integrated lab optimization and automation.

Optimize efficiency and outcomes with data-driven infectious disease management.

Connected microbiology for blood culture and ID/AST.

Visual insights into pathogen circulation trends in near real time.

Real-time instrument system support to keep your laboratory running.