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Industry News: Page 301

Regulatory
Counterfeiting drugs: Growing, global problem
European market could become portal for counterfeit drugs coming into the United States.
August 10, 2005
Regulatory
Written procedures needed for label verification
According to the regulations enforced by the Food and Drug Administration, "There shall be written procedures designed to assure that correct labels, labeling, and packaging materials are used for drug products" (21 CFR 211.130) and "Each manufacturer shall control labeling and packaging operations to prevent labeling mixups" (21 CFR820.120d). Verification of the correct labels can be simple or complex. A labeling process that utilizes preprinted labels affixed during the packaging process may require a simple verification. A more complex verification may be required for a process such as the downloading of product information from an ERP system for the on-line printing of unit labels and cartons that could include printing, reading, and verifying bar codes.
July 10, 2005
Regulatory
Bar-code anticounterfeiting system
July 10, 2005
Regulatory
Equipment qualification
July 10, 2005
Regulatory
Anticounterfeiting and antifraud products
Kevin O’Donnell, Senior Partner, Exelsius, is a noted authority in supply chain integrity. In this Q&A he lends his “big-picture” insights regarding distribution practices for time and temperature-sensitive pharmaceutical/biological products.
July 10, 2005
Supply Chain
Thoughts on FAT
If validation documentation is done earlier, the Factory Acceptance Test (FAT) can be a simple procedure, but not always. "It used to take only a couple of hours to make sure things were running properly during a factory acceptance test, but today it can take eight to 10 weeks to put the equipment and software through the necessary challenges to demonstrate that it will meet today's quality compliance standards," says Bikash Chatterjee, COO of consultancy Pharmatech Associates. "We need to make sure that the equipment will meet all the user and functional requirements, which means we spend more time at the factory where it's more efficient to fix things in the supplier's factory than on the customer's shop floor," he says. "Some customers are doing FATs in factories and are there for weeks on end," says Dave Schuh, VP of sales and marketing at MGS Machine Corp. "But the challenge is to understand the full scope of the FAT requirements, and fit it within the scope of work up front so that everyone wins."
July 10, 2005
Regulatory
More modular software could simplify validation
As smart machines become more prevalent, the process of validating the software becomes more complex. But by making the software modular, manufacturers are further easing the validation process. For instance, a packaging machine might have 20 servo axes, which all use basically the same subroutine. Instead of validating each axis performance individually, could you validate the subroutine once and be done? The manufacturer could hand over the validated modules and documentation, and the process would be complete.
July 10, 2005
Regulatory
Can templates simplify the validation process?
MGS Machine Corp., a packaging machinery OEM with a keen interest in pharmaceutical packaging, is developing templates to help its customers with the validation process. For example, for machines that attach an outsert, MGS provides a five-page template that explains in explicit terms how the machine works, how bad product is rejected from the line, how the machine communicates, and how it verifies that the reject really did happen. Also developing templates is the JETT (Joint Equipment Transition Team) Consortium, a special interest group of the International Society for Pharmaceutical Engineering, created to help ease the cGMP process. JETT aims to improve communication between users and suppliers of automated production and process equipment to meet validation requirements more effectively.
July 10, 2005
Supply Chain
PAT seeks quality by design
The pharmaceutical industry responded to the FDA's cGMP report with Process Analytical Technology, or PAT, a system to design, analyze, and control manufacturing and packaging processes through timely measurements of critical quality and performance attributes. The goal of PAT is to understand and control the processes with the assumption that quality cannot be tested into products, but rather should be built into systems by design.
July 10, 2005
Regulatory
Responding to the FDA's cGMP report
The fundamental process for validation has been in place for 10 years: The pharmaceutical company develops qualifications for a packaging machine, then passes them off to a supplier for equipment designing and manufacturing. After testing and approving the equipment, the pharmaceutical company begins operations. The Food and Drug Administration made this process at once both easier and more difficult last September with its report "Pharmaceutical cGMP's for the 21st Century – A Risk-Based Approach." Current good manufacturing practices (cGMPs), sometimes known as good automated manufacturing practices (GAMP), have long been a standard practice in the pharmaceutical industry, but new technologies and approaches to quality assurance required more flexibility—and thus more variability—in the validation process.
July 10, 2005
Regulatory
Malaysia opts for pharma hologram
A hologram, produced by Hologram Industries (HI), is now being used to authenticate pharmaceuticals throughout Malaysia.
June 10, 2005
Regulatory
Validation efforts need to incorporate machine operators
C.R.S. Ravishankar, a guest from India at IoPP's Chicago Chapter meeting May 10, offers insights into validating pharmaceutical packaging processes.
June 10, 2005
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