Designing Transfer Carts for Class 100 Conditions

Publication
Article
Pharmaceutical TechnologyPharmaceutical Technology-08-02-2003
Volume 27
Issue 8

FDA has found several pharmaceutical companies not maintaining Class 100 conditions within transfer carts. The author discusses an approach for designing a transfer cart that will satisfy such conditions.

External Link - article-66514.pdf

Articles in this issue
BIO Update
Designing Transfer Carts for Class 100 Conditions
An Update on Osmotic Drug Delivery
The Influence of Pregelatinized Starch Disintegrants on Interacting Variables that Act on Disintegrant Properties
New FDA Initiatives Aim to Spur Innovation
Interphex Serves as a Showcase for New Materials and Machines
August 2003
In the Spotlight August 2003
Recent Videos
Christian Dunne, director of Global Corporate Business Development at ChargePoint Technology
Roger Viney, PhD, chief commercial officer for ICE Pharma
Roger Viney, PhD, chief commercial officer for ICE Pharma
Drug Digest: Challenges and Triumphs in Next-Generation Biotherapeutic Development
Christian Dunne, director of Global Corporate Business Development at ChargePoint Technology
Related Content
Science laboratory test tubes, laboratory equipment | Image Credit: © BillionPhotos.com - © BillionPhotos.com - stock.adobe.com

Argobio and University of Southern Denmark Launch New Next-Gen RNA Company, Inverna Therapeutics

Feliza Mirasol
January 8th 2025
Article

Using splicing technology, the new company aims to innovate safer and more effective RNA therapies for severe genetic diseases.

Drug Solutions Podcast: Realizing AI’s Potential

Drug Solutions Podcast: Realizing AI’s Potential

Felicity Thomas
December 20th 2024
Podcast

This episode is a compilation of comments taken from a series of interviews where experts are discussing how AI might impact the global bio/pharma industry in the future.

Hand shaking which print screen on wooden cube block in front of human icon for business deal and agreement concept. | Image Credit: © Dilok - stock.adobe.com

Molex, Phillips Medisize Close Acquisition of Vectura Group

Patrick Lavery
January 7th 2025
Article

The transaction, which was first announced in September 2024, expands Phillips Medisize’s inhalation drug delivery capabilities.

Drug Solutions Podcast: Dosage Forms: Roundtable on Oral Solid Dosage Trends

Drug Solutions Podcast: Dosage Forms: Roundtable on Oral Solid Dosage Trends

Patrick Lavery
October 30th 2024
Podcast

In this podcast episode, we discuss trends in dosage forms, specifically oral solid dosage, as viewed by five industry experts who recently exhibited at CPHI Milan.

Science laboratory test tubes, laboratory equipment | Image Credit: © BillionPhotos.com - © BillionPhotos.com - stock.adobe.com

Takeda Receives Japanese Regulatory Approval for HYQVIA Subcutaneous Injection for Treating Agammaglobulinemia or Hypogammaglobulinemia

Feliza Mirasol
January 4th 2025
Article

With this approval, HYQVIA [Immune Globulin Infusion 10% (human) with Recombinant Human Hyaluronidase] becomes the first and only facilitated subcutaneous immunoglobulin available in Japan to treat these disorders.

Text sign showing Industry News. Business photo text delivering news to the general public or a target public | Image Credit: © Artur - © Artur - stock.adobe.com

FDA Releases Draft Guidance on Sampling and Testing of In-Process Materials and Drug Products

Susan Haigney
January 3rd 2025
Article

The draft guidance document provides recommendations for complying with 21 CFR 211.110.