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  • Our extensive experience in solid-state systems has led our researchers to develop specific and flexible protocols for the study of crystalline forms. These can be adapted to meet the needs of the pha...

  • PolyCrystalLine has its own research laboratory equipped with the most up-to-date advanced technology. The laboratory operates according to the Good Laboratory Practice (GLP) directives. A modular ap...

  • Quantization methods are validated in order to quantify specific crystal forms or amorphous content in API mixtures and tablets (formulated compounds). Depending on the physical-chemical API character...

  • PolyCrystalLine have specialist knowledge of optimization procedures for the various factors during the crystallization processes to achieve a viable crystal form, particle size and yield.   1....
Profile
PolyCrystalLine is a young dynamic company which has established itself as a leader in research and characterization of solid-state compounds, especially in the pharmaceutical sector. We have developed a university background into a business venture; blending academic know-how with business-like agility and flexibility. By working closely with the academic world, we are able to apply an innovativ...
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U(H)PLC ANALYSIS
Polycrystalline
PolyCrystalLine starts with new services: U(H)PLC analyses Methods development and validation using U(H)PLC technique   ICH Validation The methods developed are validated for testing scientific integrity following ICH guidelines, including preparation and validation protocols and reports....
UPGRADE WITH EASYMAX
Polycrystalline
    Experience the power of simplicity Enjoy the ease-of-use Explore the robustness  The EasyMax™ synthesis workstation redefines the way chemists do optimization of synthesis and crystallization processes.EasyMax™ allows to make correct decisions timely, and bring new products to the market faster.EasyMax™...
SCALE-UP UNTIL 20 LITERS
Polycrystalline
PolyCrystalLine opens the new laboratory dedicated to industrial processes optimization and production of small scale batches (GLP certified) of specific crystalline forms. Scale-up from 50 mL to 20 Liters scale....
In Vitro Bioequivalence Testing (BE)
Polycrystalline
The Bioequivalence study is requested to determine rate/extent of absorption of each therapeutic moiety for: –  Potential generic products for which there is a reference listed drug (RLD) approved for marketing, –  Potential new drug products (new salts, dosage forms) for which adequate clinical studies have already been con...
   
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