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Patient-Centered Controlled and Modified Release Drug Delivery: Formulation & Process Development Drug delivery challenges include frequent dosing, nighttime administration, and site-specific absorption needs. Controlled and modified-release technologies help improve bioavailability, compliance, a...
Quantitative Clinical Pharmacology (QCP)
Determination and Control of Crystal Form in ASD Formulations: A Case Study on Everolimus Tablets
API Form and Solid-State Research Crystal Pharmatech employs an integrated approach to identify and develop the best crystal form for your small molecules through effective screening and rigorous assessments.
Crystallization Development The aim of a crystallization process development is to find a crystallization process which can stable produce the optimal solid form with all desired properties such as particle size, particle shape,...
Mini-tablet Pediatric medication is a long-standing unmet clinical need in China. Taking medicine by breaking, guessing on dosage, and lack of special medicines are the main chaos in pediatric medication. From the perspective of physiology and pharmacology, they are not just "miniature versions" of adult drugs, and corresponding changes in dosage form, dosage, and administration form are required.
Accelerating Drug Development through Collaboration Molecules-to-Medicine: Accelerating Drug Development through Collaboration
Case Study 4: Gatifloxacin - Crystalline Form Changes With A Licensed Compound Gatifloxacin (also known as AM-1155, CG5501, and BMS-206584) has been established as a fluoroquinoline broad-spectrum antibiotic (Fukuda et al. 1998) (Fig. 10). It was originally discovered by Kyorin ...
Presentation
Stability and Solubility Studies Chemical and physical stability. The intent of the stability study is to evaluate the chemical and physical stability of the API in solution and solid-state. The solid-state evaluation will probe the pr...
Comprehensive Physicochemical Property Evaluation A comprehensive physicochemical property evaluation is an important premise for the development of formulation and process. It provides an important basis for the druggability evaluation of the compou...
Pediatric Formulation (Mini-tablet) The development of acceptable, palatable pediatric formulations is undergoing transformation within the industry today, driven by patient needs and regulatory requirements. Therefore, the demand for a...
Crystal Formulation Services successfully passed the dual certification of GMP and GDP conducted by SGS Recently, Crystal Formulation Services (CFS) successfully obtained dual certification in Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) from SGS, an internationally recognize...