We have 20+ years of expertize in pharmaceutical materials science
We are devoted to supporting customers within the field of solid-state characterization of particles – primarily within the pharmaceutical industry. Save time! We can assist you in all phases from drug discovery to final product manufacturing in GMP processes and we can develop all the methods you need. We offer all the standard techniques and a lot of unique analyses.
We are cGMP compliant with a certificate from the Danish authorities – and registered with the FDA.
We have a short response time, reliable service and strong costumer relations – who recommend us.
Outsource a specific analysis to us!
We will guide you in the selection of the analysis and parameters. We can support your in-house capabilities, or we can complement them.
We set up a service package according to your needs!
We will take care of all needed protocols and reports, interpret the results and discuss the conclusions with you.
Our special expertise is:
Solid-state analysis (also referred to as particle analysis/powder analysis) consists of the examination of particles sizes and of physical properties such as crystallinity, dissolution rate, stability…
Particle size is by far the most important physical property of particulate samples. Particle size determinations are routinely carried out in our laboratory.
At Particle Analytical we offer a package of analysis required to characterise a new solid API with regard to physical properties such as particle sizes and crystallinity/stability etc. Within two weeks we perform the full analysis of the compound and write a report that can be used for regulatory purposes.