Quasaar GmbH is a GMP-certified and FDA-approved analytical laboratory offering quality control of raw materials, excipients, active pharmaceutical ingredients (APIs), and medicinal products for the human and veterinary sectors.
Ensuring the efficacy and safety of the product to protect patients is our top priority.
This is complemented by a comprehensive quality assurance system designed to ensure full GMP compliance.
Paddle & Basket (USP 1 & 2) 
Franz-cell system
Analytical sieves from 125 to 1000 µmIn addition to the GMP-compliant execution of analytical methods, our service offering is complemented by a range of additional services.
You will find a detailed description of work packages such as validation, method transfer, biopharmaceutical characterization, as well as other specialized analyses under the section Contract Analytics:
What steps are required to initiate an analytical service order?
Please use the contact form below to let us know which analytical task or question you would like our assistance with.
Or contact us directly by telephone on 06826-918962-0 or request@quasaar.de
Our team will review the technical feasibility of your request based on the information provided.
We will contact you if further clarification or additional information is required.
Based on your specifications, you will receive a quotation or cost estimate.
Once you place the order, the project will begin.
Please send your test samples along with the corresponding safety data sheet (SDS) to our sample intake team.
We will review your shipment and send you a confirmation of receipt.
The analysis will then be scheduled according to the order and the agreed timeline.
We will deliver the analytical results (paper based document or electronic data in your LIMS) to you and, if necessary, arrange for the disposal of any remaining test samples.
Feel free to reach out to us by email – our GMP analytical experts will personally handle your inquiry and provide you with the support you need.