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| home > pmps > autumn 2002 > new opportunities - speciality pregelatinised starch excipients |
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 PUBLICATIONS |
Pharmaceutical Manufacturing and Packing Sourcer
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| Excipients are increasingly being recognised for the critical role they play in pharmaceutical products. Pharmaceutical excipients contribute enormously to the efficacy of a product by providing specific special functionalities in formulations. Excipients bind tablets together under the stress of direct compression, control the release of active ingredients, help tablets to disintegrate and dissolve efficiently and influence absorption. Formulators of finished dosage forms are dependent on excipient manufacturers to provide substances which are uniform in chemical and physical characteristics, offer processing benefits and meet the highest global standards. New, multi-functional, high purity excipients which comply with all regional pharmacopoeia requirements simultaneously - and can therefore be used worldwide - are now available. Here, the role of this new generation of excipients is examined with reference to their functional properties. |
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Industry Events |
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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.
More info >> |
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News and Press Releases |
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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.
More info >> |
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