Formulation Development and Clinical Supply Manufacturing
Laval, Quebec
Be Clinic Ready! Corealis Pharma provides services on a contract basis in the areas of Formulation & Process Development as well as in small scale Clinical Trial Material (Phase I and II) Manufacturing and the packaging of solid dosage forms (tablets & capsules) to pharmaceutical and biotech companies. Our services include: API characterization; salt selection; pre-formulation; formulation & process development; analytical method development; stability storage & testing; technical transfer and scale-up; cGMP manufacturing & packaging of Phase I and II CTM; dossier support for American, European, and Canadian submissions. Our experts have access to modern well equipped R&D and cGMP manufacturing & packaging facilities that allow them to successfully complete the most challenging and complex mandates. The primary objective of Corealis and its staff is to make every one of their customers succeed. Corealis Pharma Inc. offers personalized and efficient services in the areas of Formulation Development and Clinical Supply Manufacturing of solid oral dosage forms.
On-site · Laval
Perform analytical testing for pharmaceutical product development, including HPLC, titration, dissolution, stability, and physical characterization of APIs, intermediates, and finished products. Document and evaluate results, support analytical investigations, maintain laboratory supplies and equipment, and follow safety, SOP, and GMP requirements.
On-site · Laval
Perform analytical testing for pharmaceutical product development, including HPLC, sample preparation, titration, dissolution and stability testing, physical characterization, and OOS investigations. Document and evaluate results against R&D and GMP criteria, follow laboratory safety procedures and SOPs, maintain laboratory supplies and organization, and support analytical investigations.
On-site · Laval
Support oral solid dosage formulation and pharmaceutical process development, including R&D batch preparation, GMP pilot plant activities, and sourcing laboratory supplies. Characterize APIs, develop and test formulations, conduct stability studies, prepare prototypes for animal pharmacokinetic studies, and write technical reports.
