Search results Search for: Search Refine your results by duration: Any Under 5 mins Under 20 mins Over 20 mins Sort by: Relevance Views Date Using PAT to accelerate and optimize the process development Lizbeth Martinez, Ph. D, at Novartis Basel Switzerland and Emiliano Genorini, at Viavi Solutions Full Title: Using PAT to accelerate and optimize the process development of solid dosage forms. Near-infrared spectroscopy (NIRS), as one of the maj... 1 year ago | 79 mins Material Understanding for Continuous Manufacturing of Solid Dosage Forms Dr Yifan Wang, regulatory research scientist, FDA CDER and -Dirk Leister, Head of the Application team Thermo Fisher Scienti In continuous manufacturing of solid dosage forms, continued assurance of process performance and product quality is based on accurate and consistent ... 4 years ago | 68 mins The Future of Pharmaceutical Manufacturing: Flexibility and Sustainability throu Daniel O. Blackwood & Jeffrey Moriarty of Pfizer, Inc. Following a decade (or more) of concerted effort by industry, regulator, and academic groups, recent technology investments are now beginning to shape... 5 years ago | 68 mins Pharmaceutical Hot Melt Extrusion A Cost Effective Method to Increase Solubility Dennis Douroumis, of University of Greenwich and Dr.-Ing Margarethe Richter, Pharma Application Specialist at Thermo Fisher Full Title: Employing Hot Melt Extrusion As a Cost Effective Method of Increasing Solubility Of Water Insoluble API’s • Identifying the appropriate ex... 4 years ago | 59 mins Addressing Material Properties in the Design of a Direct Compression Continuous Professor Fernando Muzzio Virtually, all solid dosage forms in the pharmaceutical industry have been manufactured in ‘batch’ despite cost and processing disadvantages associate... 9 years ago | 47 mins Janssen CM-strategy: A Story of Multiple Platforms From R&D to Commercial Presented by Jeroen Geens, Engineering Technical Director at Janssen Research & Development After initial CM projects and successes for specific compounds in its commercial portfolio, Janssen defined in 2015 a vision to make continuous manufa... 2 years ago | 103 mins Using In-Vitro Dissolution to Support Post Approval Changes Global Regulatory Ex Dr Xin Bu, Principal Scientist, Bristol-Myers Squibb Dissolution is one of the critical quality attributes for solid oral dosage forms, typically tablets and capsules. In addition as a quality control (Q... 4 years ago | 43 mins Addressing Material Properties in the Design of a Direct Compression Continuous Professor Fernando Muzzio Virtually, all solid dosage forms in the pharmaceutical industry have been manufactured in ‚Äòbatch‚Äô despite cost and processing disadvantages assoc... 9 years ago | 47 mins
