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Quincy MattinglyRegional Manager - AlpVisionIn the war against counterfeits, regulators have concentrated on serialisation and ePedigree and missed an opportunity on product authentication, according to AlpVision. Published: 07-May-2013 |
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VariousVarious - VariousRisk-based monitoring for clinical trials was a hot topic at this year’s PCT Europe thanks to recent draft guidances from the FDA and the EMA. Published: 12-Nov-2012 |
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Philip Ridley-smithBusiness Development & Marketing Manager - Cobra BiologicsCMO Cobra Biologics says North America is an obvious place to look at for a facility acquisition. Published: 25-Oct-2012 |
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Kurt Nielsen and Cornell StamoranVarious - CatalentCatalent says making its technology available to industry will not affect its competitive edge. Published: 22-Oct-2012 |
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David Lyon and Karen CoppensVarious - Bend Research and DowBend Research is “actively” hunting new partnerships similar to its recent alliance with Dow. Published: 17-Oct-2012 |
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Andrea SchieferVP of European clinical operations and executive director of pharmacovigilance - ClinipaceThe proposed changes to European clinical trial regulations accepted by the European Commission (EC) in July will put Europe on an equal playing field, according to Clinipace’s Andrea Schiefer. Published: 21-Aug-2012 |
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Gareth WilliamsUK director of market access - QuintilesNegotiating funding for drugs with local health authorities prior to commercialisation is the key to success for biopharmas working in the changing European market, says Quintiles. Published: 07-Jun-2012 |
Sue MackayResearch nursing team manager - ResearchNurses.coThe use of home visits in clinical trials could raise the chances of regulatory approval, according to ResearchNurses.co. Published: 31-May-2012 |
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Sue MackayResearch nursing team manager - ResearchNurses.coIncluding home visits in clinical trial designs could be the key to patient retention, according to ResearchNurses.co. Published: 30-May-2012 |
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Zoran AntonijevicSenior director of the centre for statistics in drug development and innovation in the US - Quintiles‘CROs: look at the entire portfolio, not just the individual project, when planning clinical studies,’ says DIA’s adaptive design scientific working group. Published: 22-May-2012 |
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Eric HoffmanVP Business development and marketing - North America - SGS Life Science ServicesSGS has added formulation development to its service offering through the expansion of its laboratory in Illinois. Published: 07-May-2012 |
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Aiswariya ChidambaramMarket Analyst - Frost & SullivanThe European CMO industry could be blocked by over complex layers of regulation, says Frost & Sullivan analyst Aiswariya Chidambaram. Published: 25-Apr-2012 |
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Rahlyn GossenOwner - Rebar InteractiveDesigning trials around patients’ habits is the key to success in patient compliance, according to online recruitment specialist Rebar Interactive. Published: 16-Apr-2012 |
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VariousVarious - DIA EuromeetingThose seeking leadership positions in the pharmaceutical world should take to social networking sites to get noticed, recruitment specialists say. Published: 10-Apr-2012 |
VariousVarious - DIA Euromeeting, 2012Regulatory reform was the name of the game at this year’s DIA Euromeeting in Denmark. Published: 05-Apr-2012 |
Carolyn FinkleVP of global regulatory consulting - CatalentCatalent wants to build on its European expansions by replicating the end-to-end drug development services model in emerging markets. Published: 04-Apr-2012 |
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Peter GeorgeCEO - Clinigen GroupSourcing comparator drugs for trials is a complex ‘art’ that requires knowledge of trading, regional regulations and an awareness of drugmakers’ competitive concerns according to Clinigen Group CEO Peter George. Published: 27-Mar-2012 |
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Hedley ReesIndustry consultant - Biotech PharmaflowPlanning supply chains early is an important part of maintaining margins but is often overlooked by Pharmas too focused on developing the next product in an era of patent expiry says industry consultant. Published: 26-Mar-2012 |
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Aiswariya ChidambaramHealthcare market analyst - Frost & SullivanThe European CMO sector is set to double in the next six years and will hit revenues of up to $20.75bn, according to Frost & Sullivan’s Aiswariya Chidambaram. Published: 15-Mar-2012 |
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Jamie BlackburnFounder - Patient NucleusPharma companies must become more involved in building patient communities through social media if they want to see a successful trial recruitment process according to Patient Nucleus founder Jamie Blackburn. Published: 27-Feb-2012 |
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Julian HanakCommercial director - Cobra BiologicsDetailed market knowledge and an experienced CMO are still critical to successfully developing a biopharmaceutical or biosimilar according to Cobra Biologics. Published: 25-Jan-2012 |
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Patricia LeuchtenCEO - The Avoca GroupSponsor and CRO perceptions of the quality of outsourced service provision differ markedly according to a study by consulting and survey research organisation, the Avoca Group. Published: 08-Dec-2011 |
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Thomas EldredCEO - RecipharmThe global contract manufacturing market may be showing signs of recovery but careful investment and focusing on core activities is still the most sensible approach according to Sweden-based CDMO Recipharm. Published: 05-Dec-2011 |
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Joseph CameroExecutive recruiter - RPSContract services providers which embed service personnel in pharma companies are becoming more prominent in the industry. Published: 21-Nov-2011 |
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David DowneyVP Commercial Operations - Almac Pharma ServicesAlmac says growing demand for non-GMP manufacturing work rather than competition was the key driver for expansion of its product development services business. Published: 15-Nov-2011 |
BioPharm America™ 2013—6th Annual International Partnering Conference
Boston, MA, USA / Conference