PharmTech
5 days ago · A genetic medicines customer has selected the company’s binders for commercial development of the customer’s product. 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
Certificates of Analysis: Don’t Trust, Verify - PharmTech
Apr 2, 2018 · Certificates of analysis (CoAs) are a tangible, and important, manifestation of a manufacturer’s relationship with its suppliers of APIs, excipients, and the other materials used to make drug products. Provided by suppliers to customers as a matter of course, these documents operate at the point where materials, laboratory control systems ...
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.
Orally Disintegrating Tablets - PharmTech
Oct 2, 2005 · Over the past three decades, orally disintegrating tablets (ODTs) have gained much attention as a preferred alternative to conventional oral dosage forms such as tablets and capsules. An ODT is a solid dosage form that disintegrates and dissolves in the mouth (either on or beneath the tongue or in the buccal cavity) without water within 60 ...
Deviation Investigation Format and Content: A Guide for
Jul 2, 2017 · History review. The history review section is intended to provide the reader with an overarching historical context of the deviation event. This section typically includes a query of the quality management system with specific words and phrases pertaining to the current deviation event with the goal of identifying similar and/or related events.
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 ...
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.
Choosing Capsules: A Primer - PharmTech
Oct 2, 2017 · Choosing Capsules: A Primer. Published on: October 1, 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.