Pharmaceutical Technology - PharmTech
WEBThe Real Message Behind Commercial mRNA Products, April 2023 eBook
PharmTech | Page 10
WEBMar 21, 2024 · CordenPharma Expands Clinical Peptide Capacity. March 06, 2024. The company is expanding GMP capacities at its Frankfurt site to manufacture early clinical-phase peptide APIs. Pharmaceutical Technology is the independent source for information, insight, and analysis on bio/pharmaceutical formulation, development, and …
Best Practices for Designing and Building a Pharmaceutical ...
WEBFeb 2, 2021 · Best Practices for Designing and Building a Pharmaceutical Manufacturing Facility. Pharmaceutical Technology, Pharmaceutical Technology-02-01-2021, Volume 2021 Supplement, Issue 1. For drug sponsors that are considering building their own manufacturing facilities, an expert project team is crucial. To achieve delivery of a facility …
Planning and Designing a Pharmaceutical Facility: A Process
WEBSep 1, 2005 · This first article discusses some of the ways in which experienced external service providers can add value to the early stages of pharmaceutical facility planning and design by providing. an independent and objective viewpoint. methods and experience to analyse the process as a whole. modelling and simulation tools. benchmarking data.
Pharmaceutical Technology Submission Guidelines and
WEBJul 31, 2020 · Pharmaceutical Technology and Pharmaceutical Technology Europe magazines set the standard for publishing independent, industry-leading information on the technologies, strategies, and regulations crucial to professionals developing and manufacturing pharmaceuticals and biopharmaceuticals.. The editorial mix of peer …
All Whitepapers | Page 3
WEBAdvancing Lipid-Based Formulations and Softgels in Drug Development (Feb 2024) February 22, 2024. Lipid-based formulations (LBFs) are complex mixtures of lipid, surfactant and solvent excipient, wherethe composition determines the potential impact of dispersion and digestion on drug solubilization. By carefullyselecting fill formulations …
Practical SPC Rules in the Real World of an Ongoing Process ...
WEBOct 3, 2021 · The European Union (EU) good manufacturing practice (GMP) and FDA regulatory documents require manufacturers to monitor pharmaceutical and biopharmaceutical product quality to ensure that a “state of control” is maintained throughout the lifecycle of new and legacy products during the third process validation …
Data and the Supply Chain - pharmtech.com
WEBAug 12, 2020 · Data and the Supply Chain. The COVID-19 pandemic has highlighted the challenges and complications of sourcing, tracking, and testing materials for pharmaceuticals. Pharmaceutical Technology spoke with Joe DiMartino, Luminata solution manager at ACD/Labs about the impact COVID-19 is having on the pharmaceutical …
New Technologies Enhance the Formulation of Highly Potent …
WEBOct 2, 2014 · New encapsulation technologies. Evonik has developed the FormEZE technology, an improved microencapsulation process for the manufacture of PLG microparticles. The continuous, closed-equipment process involves an emulsion-based extraction and affords 20% higher yields with less post-process handling, according to Tice.
Keys to Executing a Successful Technology Transfer - PharmTech
WEBFeb 1, 2011 · Keys to Executing a Successful Technology Transfer. Published on: January 31, 2011. Ian Uydess, Wiliam Schmidt. Pharmaceutical Technology, Pharmaceutical Technology-02-01-2011, Volume 2011 Supplement, Issue 2. The authors highlight the need for a technology-transfer process that is efficient, cost-effective, and repeatable, …
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