PharmTech
2 days ago · Out-of-the-Box Packaging Advancements. Pharmaceutical packaging must advance to adapt to new, complex modalities. Pharmaceutical Technology is the independent source for information, insight, and analysis on bio/pharmaceutical formulation, development, and …
The Basics of Aseptic Processing - PharmTech
Oct 2, 2021 · A. Aseptic processing is a manufacturing method that can produce product that is absent of bacteria without subjecting the product to terminal sterilization processes. Many products degrade and become ineffective when subjected to the harsh conditions of terminal sterilization. Aseptic process manufacturing allows these products to be produced ...
Pharmaceutical Technology - PharmTech
The Real Message Behind Commercial mRNA Products, April 2023 eBook
Best Practices for Designing and Building a Pharmaceutical ...
Feb 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 that ...
Understanding USP Water for Pharmaceutical Use - PharmTech
May 1, 2017 · Understanding USP Water for Pharmaceutical Use. The type of water for pharmaceutical use is determined by USP testing. Manufacturing of pharmaceutical products, medical devices, biologics, cell- and tissue-based products, and many other medical products requires significant volumes of water. Water is more complicated than what most people think.
Deviation Investigation Format and Content: A Guide for
Jul 2, 2017 · Pawel Drapala. Pharmaceutical Technology,Pharmaceutical Technology-07-02-2017, Volume 41, Issue 7. Pages: 108–110. This article presents a general strategy for authorship of deviation investigations, with primary focus on regulatory inspection success. The primary purpose of a deviation investigation report in a GMP environment is to clearly ...
Classifying Potent and Highly Potent Molecules - PharmTech
Aug 1, 2018 · This variability in classification is exemplified by a study carried out by Cambrex in which a panel of 38 molecules was sent to three risk assessors. Three different results were provided: one assessor deemed five of the 38 to be highly potent, one assessed 37 of the 38 to be highly potent, and the third fell somewhere between the two extremes.
The Fundamentals of Dissolution Testing - PharmTech
Oct 2, 2019 · The primary functions of a dissolution test during early stages of development are to characterize therapeutic efficacy, bioequivalence, and bioavailability of API. During later stages of the development process, dissolution testing is also used for quality control (QC) purposes. “The type of dissolution testing performed along with the ...
Choosing Capsules: A Primer - PharmTech
Oct 2, 2017 · Choosing Capsules: A Primer. Published on: October 2, 2017. Milind K. Biyani. Pharmaceutical Technology,Pharmaceutical Technology-10-02-2017, Volume 41, Issue 10. Pages: 36–41. Capsules offer certain benefits over tablets for oral-solid dosage drugs, and several types of capsules are available. Oral-solid dosage (OSD) drugs can be formulated ...
PharmTech
Genentech Enters an Approximately $2 Billion Deal to License Sangamo Therapeutics Technologies for Developing Neurodegenerative Disease Therapeutics. August 20th 2024. Genentech will have access to Sangamo’s capsid delivery platform and epigenetic regulation capabilities to develop genomic medicines for certain neurodegenerative diseases.