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European BioPharmaceutical Review

In Biotech, Saxony Matters

In times such as these, when almost every hamlet with a stop sign claims to be a biotechnology cluster, it is hard to distinguish which bioregions are worth taking seriously in terms of their real offerings and, perhaps more importantly, their likelihood of survival. biosaxony, the biotechnology region in Saxony, Germany, is a serious cluster, and one that takes these issues to heart. Although criticised for being a late-comer, biosaxony has capitalised on the mistakes of other earlier ventures into the cluster world and distinguished itself right from the start by not becoming just another cluster, but a total concept.

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By Dr Tatiana Kassessinoff, Senior Project Manager at Biopolis Consultants GmbH

Dr Tatiana Kassessinoff studied Chemistry at University College London and received her PhD in Medicinal Chemistry/Immunology in 1990. She then accepted a Fogarty fellowship award and performed five years of postdoctoral and independent research at the National Institutes of Health, USA. Since moving to Germany in 1996, Dr Kassessinoff has specialised in Scientific Communications serving the Rhein-Neckar biotechnology region, including assisting German scientists and physicians in successfully presenting themselves to the international community. More recently, she held the position of Manager of Scientific Documentation at LION bioscience AG, Heidelberg, Germany, until joining Biopolis Consultants in May 2003.

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Dr Tatiana Kassessinoff
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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 Product Development Group, Inc

HOLLYWOOD, Fla. – Azopharma Product Development Group, Inc. (“Azopharma”) announced today the addition of innovative state-of-the-art equipment at its formulation and manufacturing division, ApiCross Drug Delivery Technologies in Hollywood, Florida. The most recent acquisition is the MG Futura Capsule Filler which delivers the latest in capsule filling technology. The company has also added a Bausch & Strobel Aseptic Filling Isolator, equipment that is ground-breaking in the powder filling process. These additions support our previously implemented XcelodoseTM powder micro-dosing system. With these technologies, Azopharma is able to provide its clients with all forms of the capsule filling process. The new equipment is part of Azopharma’s recent manufacturing expansion which includes 17 new manufacturing suites for GMP, cytotoxic and aseptic products...
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