Reset Map141, President Kennedy Montreal Quebec H2X 3Y7 CanadaCOREALIS Pharma is a CDMO offering formulation development and clinical drug product material manufacturing services to pharmaceutical and biotech companies. Specialized in oral solid dose formulations, our state-of-the-art laboratories and manufacturing facilities allow our experts to successfully complete the most complex formulation scale up projects. COREALIS Pharma's goal is to provide complete satisfaction to all Clients by ensuring high quality services and delivering compliant, phase appropriate drug products on time, every time. Services provided include: API-API compatibility study Drug-Excipient compatibility study Formulation development immediate release, extended released, API-In-Capsule, Capsule, spray dried intermediate Manufacture prototype formulation for PK study R&D Stability study Formulation and manufacturing process scale-up Manufacture of clinical trial material Analytical method qualification phase 1-2 Release testing GMP stability Analytical Services XRPD SEM TGA DSC Water Content (Karl Fisher) Assay4 Related Substances4 Disintegration - one stage/ two stages Hygroscopicity (DVS) Stress test, grinding and compressibility (XRPD) Laser Diffraction Optical Microscopy Clemex Analysis Compressibility Bulk and tap density/ flow properties Forced degradation (acid, base, heat, photolytic, and oxidation)
200 Boul Armand Frappier Laval, Québec, H7V 4A6 CanadaCOREALIS Pharma is a CDMO offering formulation development and clinical drug product material manufacturing services to pharmaceutical and biotech companies. Specialized in oral solid dose formulations, our state-of-the-art laboratories and manufacturing facilities allow our experts to successfully complete the most complex formulation scale up projects. COREALIS Pharma's goal is to provide complete satisfaction to all Clients by ensuring high quality services and delivering compliant, phase appropriate drug products on time, every time. Services provided include: API-API compatibility study Drug-Excipient compatibility study Formulation development immediate release, extended released, API-In-Capsule, Capsule, spray dried intermediate Manufacture prototype formulation for PK study R&D Stability study Formulation and manufacturing process scale-up Manufacture of clinical trial material Analytical method qualification phase 1-2 Release testing GMP stability Analytical Services XRPD SEM TGA DSC Water Content (Karl Fisher) Assay4 Related Substances4 Disintegration - one stage/ two stages Hygroscopicity (DVS) Stress test, grinding and compressibility (XRPD) Laser Diffraction Optical Microscopy Clemex Analysis Compressibility Bulk and tap density/ flow properties Forced degradation (acid, base, heat, photolytic, and oxidation)
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We believe that every researcher across the world should be able to connect with the thousands of global CROs that exist and have the opportunity to work together. Like many industries,the life science supply chain has been disrupted over the last year. But there are many other circumstances such as international customs regulations or sensitive shipping times that create limitations around which countries are feasible to partner with. Sometimes, finding a CRO based in a country that best suits your research needs is imperative. We hope this contract research map allows you to find the right partner in the right place at the right time.
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