Ron Scarboro, Azurity Pharmaceuticals, explains how cross-functional development, disciplined reformulation, and post-approval metrics can help proven medicines work in everyday use.
|Articles|April 2, 2020
- Pharmaceutical Technology-04-02-2020
- Volume 44
- Issue 4
Custom-Built Heated Storage Vessel
The 20,000-gallon storage vessel from Ross Engineering measures at 10.5-ft outer diameter x 30-ft. long and is designed for product storage under atmospheric pressure at 200 ºF; it is UL-142 rated.
The 20,000-gallon storage vessel from Ross Engineering measures at 10.5-ft outer diameter x 30-ft. long and is designed for product storage under atmospheric pressure at 200 ºF; it is UL-142 rated. The stainless-steel vessel comes equipped with a 32-in. manway with davit for easy access to an internally supported insertion heater, along with nozzles, saddles, and lugs as specified by the end user. The vessel is also blasted and painted with black primer for outdoor exposure.
Articles in this issue
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Biosimilars Poised for Gains in US Marketover 6 years ago
Critical Knowledge for Preparing Auditsover 6 years ago
Can Vaccine Development Be Safely Accelerated?over 6 years ago
Supercritical Fluid Chromatography Systemover 6 years ago
Quaternary Diaphragm Pumpover 6 years ago
Well Plates and Cartridges for Liquid Extractionover 6 years ago
Alternative Cleaning Validation Methods for Biologicsover 6 years ago
Pharma’s Leadership Role in a PandemicRelated to this article
The FDA approves oral pritelivir for drug-resistant herpes sores in immunocompromised patients; what it means for antiviral development and manufacturing.
This week, drug formulation and manufacturing experts showcased their knowledge, and companies exhibited their products, at CPHI Milan.
FDA approves Teva’s Weltruza, a once-monthly subcutaneous olanzapine for schizophrenia whose copolymer depot eliminates post-injection monitoring.
Equivalence test using two one-sided tests are widely used for demonstrating the comparability of treatment effects in different research fields. The method described in the manuscript aims to use simulations in Microsoft Excel to compute power for 2 one-sided tests for two groups with unequal variances.
Richard Jaenisch examines whether FDA's NAM pathway truly shortens drug pipelines or just shifts the evidentiary burden elsewhere.
Susan J. Schniepp, distinguished fellow with Nelson Labs, and Siegfried Schmitt, PhD, vice president, Technical, with Parexel, clear up some of the confusion about what does and does not need to be complied with regarding standards set by international pharmacopoeias.
Mitigating nitrosamine risk requires assessing each product individually, says Bram Baert, Global Head of Regulatory Affairs at Capsugel, and Sandrine Picco, Senior Analytical Specialist on Capsugel's Innovaform Accelerator Team, in this interview with PharmTech.