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Pharmaceutical Manufacturing and Packing Sourcer

Eliminating Waste and Adding Value

A Look at Pharmaceutical Manufacturing and Packing Processes

Waste and How it Damages your Company

When you read the word 'waste', what do you think this means to you and the business you work for or maybe own? Have you considered all the forms of waste that can effect the quality, delivery schedule and cost of your products, and ultimately your bottom line? In today's increasingly competitive climate, can you afford not to make the maximum effort to eradicate waste from your company? Moreover, given the increased pressure on your company's margins, can you eliminate waste without having to resort to the risks associated with increasing expenditure on new capital equipment which makes heady promises to increase machine throughput by x% and machine capacity by y%?

This is a conundrum facing many manufacturers; and all of these manufacturers, encompassing all sectors, from packaging manufacture to food processing to process industries, can look towards lean manufacturing principles and philosophy as a means by which they can gain that competitive edge and ensure sustainable growth in the future.

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By Daniel Nash, Manufacturing Advisor at London Manufacturing Advisory Service

Daniel Nash has a BEng degree in Manufacturing Systems with Business from Kingston University and has worked in both the automotive supply and electronics industries. He began his career working for a manufacturer of pumps for the automotive industry. He then went on to work for an industrial Ni-CD battery manufacturer, before moving to a supplier of industrial standby power systems to the UK market. He is currently working as a Manufacturing Advisor, where he assists manufacturers through the London Manufacturing Advisory Service.

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Daniel Nash
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Industry Events

4th Annual Patient Recruitment and Retention in Clinical Trials

13-15 October 2008, Amsterdam

Patient recruitment is now consuming thirty percent of clinical trial time - more time than any other clinical trial activity - and almost half of all trial delays result from patient recruitment problems. As the recruiting culture becomes more sophisticated and the forces affecting patient enrollment grow more numerous and complex, pharmaceutical companies are striving to discover new strategies to facilitate enrollment in clinical trials. With increasing industry pressure to develop, test and market greater numbers of new drugs faster, pharmaceutical companies need to perform clinical trials as quickly as possible. Inefficient patient recruitment processes is a formidable barrier to pharmaceutical companies' success in launching new products. Improving the patient recruitment process is imperative to avoid wasted investments and eliminate costly delays in bringing new drugs to market -- today and even more so in the not-so-distant future. Improved patient recruitment presents one of the largest opportunities for pharmaceutical companies to eliminate delays in clinical trials, thereby making it possible to reduce time to market.  With patent time limits and large overheads meaning that any delays in the development timeline can be disastrous, a good understanding of how to successfully recruit patients for trials is vital for any company looking to succeed.
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News and Press Releases

Azopharma Announces Plans to Implement XcelodoseTM Technology in the Production of Early Stage Clinical Trial Materials

HOLLYWOOD, Fla. – Azopharma Product Development Group, Inc. (“Azopharma”) announced today plans to implement Xcelodose technology at its formulations development facility, ApiCross Drug Delivery Technologies. Xcelodose technology is a powder micro-dosing system developed by Meridica. This technology offers a unique powder dispensing system for small-scale capsule filling and ultimately assists in conserving valuable research material as well as reducing various Preformulation activities.
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