Pharmaceutical Engineering July/August 2019 Cover

Downloads

Improving Pharmaceutical Connections with Patients

Cover: Delivering pharmaceutical solutions to patients may be more effective with new developments in digital delivery and tracking. This follow-up on a presentation at the 2018 ISPE Annual Meeting & Expo explores some trending solutions.

Application of the Soc 2+ Process to Assessment of Gxp Suppliers of It Services

Feature: To facilitate the assessment and mitigation of compliance risks associated with a third-party service organization, its services, and the systems used to provide the services, this article proposes adopting an approach from the financial sector that, with a little modification, could be used to assess suppliers of GxP-regulated IT services.

The Digital Twin: Creating Efficiencies in a Virtual World

Feature: This article on the digital twin (a virtual replica of a physical entity) launches an ongoing series from the Pharma 4.0 Special Interest Group focusing on key technologies that will modernize pharmaceutical manufacturing and facilitate digital transformation. Pharmaceutical companies use the digital twin to create and model manufacturing processes and enable analysis of how a drug will work inside the human body.

2019 ISPE Aseptic Conference: Interactive Regulatory Panel Addresses Multiple Aseptic Issues

Feature: A group of US FDA panelists responded to a range of questions from 2019 ISPE Aseptic Conference attendees on topics from restricted access barrier systems to smoke studies and artifi cial intelligence.

Accelerated Pharmaceutical Product Development, Registration, Commercialization, and Life Cycle CMC Lessons, Part 1

Feature: This article, the first of a two-part series, looks at challenges that chemistry, manufacturing, and control (CMC) development teams may encounter when a project is given accelerated development status. Key considerations and themes are introduced and future opportunities are explored.

In This Issue

Features

Being on the cutting edge of drug development is the goal of most pharmaceutical companies, but a new drug won’t work if the patient doesn’t take it. It’s a vexing problem that developers of healthcare technologies hope to address.

Features

To facilitate the assessment and mitigation of compliance risks associated with a third-party service organization, its services, and the systems used to provide the services, this article proposes adopting an approach from the financial sector that, with a little modification, could be used to assess suppliers of GxP-regulated IT services.

Features

This article is Part 1 of a two-part series exploring what we can learn from examples of pharmaceutical products being approved using accelerated programs. The series focuses on challenges that chemistry, manufacturing, and control (CMC) development teams may encounter when a project is given accelerated development status. Part 1 introduces key considerations and themes in general terms and...

Technical

The unavailability of a backup pharmaceutical water system has been a severe limitation for pharmaceutical manufacturers. Until recently, qualification concepts that adhered to current Good Manufacturing Practice (GMP) guidelines hindered the rapid setup of a water system. A new, tailor-made qualification concept for mobile water treatment has been developed to align with guidance from various...