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SIRO ClinPharm Partners with European Regulatory Expert

Thursday, September 24, 2009 09:26 AM

Indian CRO SIRO Clinpharm partnered with UK-based regulatory consulting firm Cambridge Regulatory Services (CambReg) to offer full regulatory services to clients conducting clinical trials in Europe. Services include the preparation of clinical trial applications, marketing authorizations, specialist paediatric investigation plans and paediatric use marketing authorizations.

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Ecron Acunova Founder Steps Down

Friday, April 24, 2009 08:29 AM

Ecron Acunova, a CRO based out of Germany, India and the United States, appointed Antal Hajos managing director and CEO Europe, replacing ECRON founder and CEO Klaus Wiedey, who will serve as an advisor to the company. In his new role, Hajos will oversee all business, strategic and operational aspects of the European operations. Prior to joining Ecron Acunova last year, Hajos was director of global clinical operations with Altana Pharma and later CEO of Altana/Nycomed’s research and development center and Indian affiliate in Mumbai, India.

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Start-up Spaulding Clinical Thrives Despite Economy

Thursday, March 19, 2009 08:00 AM

Late last year may not have seemed like the best time to launch a new business but that’s exactly what Randy Spaulding did when he opened the doors to Spaulding Clinical in West Bend, Wisc., in August.

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December 17

Medici Global says its Alzheimer's Facebook page demonstrates the need for more early detection trials

Analysts: Expect more equity purchases of CROs in 2013

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January 2013

Parexel celebrates 30 years of change, growth
CRO's founder and chairman reflects on challenges of the past, present and future

Strategies for increasing patient diversity in trials
Sponsors look to improve racial, ethnic recruitment without going overseas

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December 2012

Publicity, regulation tightening reins on use of KOLs
Debate rages over need to revamp how sponsors use, pay medical experts

Time may be right to makeover the investigator brochure
Size, complexity prevent critical document from being thoroughly read

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