| Following the completion of remediation efforts to deal with an FDA warning letter, Chris Phillips, AMRI's senior director of its Burlington, Massachusetts site, discusses what he considers to be a "new bar" in enforcement activity from the agency since 2009. Published: 02-May-2013 |
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The working year is almost done, time to pause from ‘the business’ and embrace the festive season…go on, give it a big hug. Happy holidays! Published: 19-Dec-2012 |
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Alan RaymondSales & Marketing Director - Aesica PharmaceuticalsUK CMO Aesica Pharmaceutical says that working with academia to access cutting edge technologies is critical for contractors that want to meet the demands of the modern drug industry. Published: 06-Dec-2012 |
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Tom SalusAssociate Vice President, Business Development - Contract Services - WockhardtWockhardt sees the ‘fractured CMO space’ as providing opportunities for growth, diversification and greater capacity utilisation. Published: 14-Jun-2012 |
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Christian AhlmarkDirector of corporate development - KemwellKemwell is set to complete a new biologics manufacturing facility in Bangalore, India, following its long-term partnership with Boehringer Ingelheim. Published: 29-May-2012 |
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Geoff GlassExecutive VP of global sales and marketing - PatheonPatheon has launched a new consulting service designed to give emerging biotechs and pharmas a boost in their drug development efforts. Published: 15-May-2012 |
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Ravi HarapanhalliPrincipal Consultant and Practice Lead for Late Stage Product Development Parexel Consulting - ParexelElectroporation is the wave of the future for transdermal drug delivery, according to Parexel’s Ravi Harapanhalli. Published: 22-Dec-2011 |
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Peter ScholeVP, pharmaceutical sciences - Quotient ClinicalQuotient has stressed the importance of screening prototype formulations early in the development process to ensure efficient drug delivery in later phases. Published: 13-Dec-2011 |
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Ray KaiserChief Scientific Officer, Biotechnology - CovanceCovance is adding mass spectrometry and other capabilities to meet growing demand for biosimilar comparability services. Published: 23-Nov-2011 |
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Mark KontnyPresident, Global Pharmaceutical Development Services - PatheonPatheon is considering buying unique drug delivery technologies to expand its development service capabilities. Published: 14-Nov-2011 |
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Scott HoultonPresident, Development and Clinical Services - CatalentCatalent is considering acquisitions as it adds scale, drug delivery technologies and capacity in emerging markets. Published: 07-Nov-2011 |
Brian O’Dwyersenior VP for global bioanalytical services - IconIcon will this year focus its R&D efforts on gaining new grounds in genomics, said Brian O’Dwyer.Icon Published: 31-Oct-2011 |
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Terry NovakPresident - Norwich PharmaceuticalsNorwich Pharmaceuticals has expanded its pilot scale production capabilities at its CDMO plant in New York, US. Published: 27-Oct-2011 |
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Luke Dimasimarketing manager - NovozymesNovozymes has achieved a successful supply chain and risk mitigation strategy through implementing its own policy with chemicals company SAFC, says Luke Dimasi. Published: 26-Sep-2011 |
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Gilles CottierPresident - SAFCSAFC announced its new aggressive growth strategy, including plans to expand in the developing markets, at its conference in Irvine, Glasgow last week. Published: 19-Sep-2011 |
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Cynthia KleppingerMedical Officer, Division of Scientific Investigations - CDER, FDAThe US FDA has warned that rapid patient enrolment in emerging markets can overload sites that lack the staff to oversee data as it is generated. Published: 18-Aug-2011 |
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Jay UdaniCEO - Medicus ResearchSystemedicus has developed informed consent and patient compliance apps for iPads and iPods and is looking to license the tools to CROs and sponsors. Published: 08-Aug-2011 |
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Ann Meeker O’ConnellActing Associate Director of Risk Science, Intelligence & Prioritization - FDAThe FDA is emphasising the key role both sponsors and CROs play in ensuring high quality clinical trials. Published: 03-Aug-2011 |
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The Big Pharma CRO strategic partnering model, its impact on drug development and the contract research sector was a hot topic at DIA 2011. Published: 02-Aug-2011 |
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In June global drug giant Pfizer began what it described as the world’s first ‘virtual trial’ using mobile technology to collect data from patients in their own homes rather than at research sites. Published: 27-Jul-2011 |
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Paula Brown StaffordPresident, Clinical Development - QuintilesUS CRO Quintiles says that demand for rapid access to clinical trial data is driving the development of vendor neutral management systems. Published: 13-Jul-2011 |
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Geoff Fatzingerdirector of regulatory affairs and strategic product development - INC ResearchCash-strapped countries are making biopharm consider a product’s fiscal benefits earlier in development, according to INC. Published: 12-Jul-2011 |
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Joshua Schultzcorporate VP of strategic account leadership - ParexelParexel says strategic partnerships let pharmaceutical companies streamline how they work with contractors and are changing how CROs view outcomes. Published: 07-Jul-2011 |
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Stewart BielerCOO - SynteractSynteract says the use of non-validated data systems in clinical trials is a key driver for the ‘rescue study’ segment of the contract research sector. Published: 06-Jul-2011 |
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James PuseyCEO - Theorem Clinical ResearchRebranded CRO Theorem Clinical Research talks about life as an independent organisation and the current vogue for private equity investments. Published: 05-Jul-2011 |