Online Exclusives
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Clinical Trials | Facilities | Logistics
Cryoport Tackles Market Needs with New NJ Facility
Contract Pharma spoke with Cryoport’s CEO, Jerry Shelton, on the reasons behind the new Global Logistics Center's launch11.02.18
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Biologics, Proteins, Vaccines | cGMP Manufacture
BioContinuum and Next Gen Processing
Andrew Bulpin of MilliporeSigma discusses key market trends and the evolution toward next generation processingKristin Brooks, Contract Pharma 11.01.18
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Trends in Biologics Manufacturing from Drug Substance to Fill/Finish
As the biologics market grows, the demand increases for development and manufacturing capabilities.11.01.18
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Anti-Cancer Evaluations with ICH S9 Guideline: What you need to know
Highlighting a few key questions from the ICH S9 Guideline Q&A documentDr. Robert Turcan, Head of Program Development, Envigo 10.26.18
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Drug Development | Information Technology
IT Alliance Aims to Overcome Early Research Challenges
Accenture, Merck and Amazon Web Services launch informatics platform for pharma researchKristin Brooks, Contract Pharma 10.08.18
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Logistics | Process Validation | QA/QC
Nulogy Launches Quality & Compliance Solution
Capabilities provided to contract packagers are purpose-designed for compliance and GMP compatible and unique to the market10.04.18
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Bio News | Collaborations & Alliances | Industry News
Sherpa Details Added Benefits After PCI Acquisition
Sherpa Clinical Packaging’s President, Mark Paiz, shares the added benefits the acquisition brings PCI's customers09.21.18
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cGMP Manufacture | Clinical Trial Materials | Clinical Trials | Drug Development
Integrating CDMO and CRO Services
Mark Egerton explains the importance of integrating formulation development and adaptive manufacturing with clinical researchKristin Brooks, Managing Editor 09.04.18
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Facilities | Inspections | QA/QC | Regulatory Affairs
Are Indian Generic Firms Improving Compliance?
Indian firms take the generics battle to U.S. turf.S. Harachand, Contributing Editor 08.09.18
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Drug Development | Regulatory Affairs
Why Otsuka Outsourced Regulatory Affairs
How outsourcing regulatory affairs gave Otsuka flexibility to move products through the development process faster.Kristin Brooks, Managing Editor 08.09.18
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Analytical Services | Bio News | Breaking News | Clinical Trials | CRO News | Drug Discovery | Laboratory Testing
Streamlining the Clinical Process
Richard Young, vice president at Veeva, shares insight on what companies can do to further expedite the clinical process07.12.18
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Biologics, Proteins, Vaccines | Drug Development
Recent Merger Creates New Cell Therapy CDMO
Dr. Pascale Bouillé of Flash Therapeutics discusses advances in the cell therapy industryKristin Brooks, Managing Editor 07.02.18
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Career Development Velocity Is Mostly Due To Random Chance
Is success in the workplace based more on factors of providence than personal qualities?Ben Locwin, Contributing Editor 06.07.18
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Clinical Trials | Drug Development
CRO Perspectives: PAREXEL
Sy Pretorius addresses trends, what is and isn’t working well in partnership models, and where the industry can improveKristin Brooks , Contract Pharma 06.01.18
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Bio News | Drug Development | Drug Discovery | Facilities | Industry News
Maximizing Discovery & Innovation While Minimizing Cost
Amrit Chaudhuri, founder & CEO of Mass Innovation Labs, shares insight on the company's inspiration & missionBetsy Louda, Associate Editor 05.31.18
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Bio News | cGMP Manufacture | Facilities | Industry News
Ecolab Details Ongoing Expansion & New Facility
The 3,000 sq ft ISO 5- & ISO 7-certified cleanroom production area will be housed within the new 12,000-square-foot facilityBetsy Louda, Associate Editor 05.24.18
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Clinical Trials | Drug Development
CRO Strategies: ICON Perspective
ICON's Nuala Murphy discusses outsourcing in today’s market, overcoming challenges, and partnership modelsKristin Brooks, Contract Pharma 05.21.18
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Regulatory Affairs | Serialization
Serialization Readiness: A contract services provider perspective
The serialization challenge and why some contract service providers and brand owners are skeptical of each other's readinessTim Wright, Editor 05.18.18
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Clinical Trials | Drug Development
CRO Trends: IQVIA Perspective
IQVIA’s Richard Staub discusses R&D trends, opportunities, challenges and collaborationsKristin Brooks, Managing Editor 05.14.18
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Clinical Trials | Drug Development | Information Technology
Accelerating Drug Development through Global Health Networks
Pfizer joins TriNetX to harness real world data for trial optimization; Manfred Stapff talks challenges and opportunitiesKrisitn Brooks, Contract Pharma 05.07.18
