
ABOUT CENCORA PHARMALEX
Beginning in January 2024, companies in the PharmaLex family started a journey of rebranding aligned with Cencora, our parent company and a leading global pharmaceutical solutions organization centered on improving lives around the world.
PharmaLex adds to Cencora’s expanding suite of pharma solutions and serves the pharma, biotech, and medtech industries. We guide clients from early strategic planning activities and non-clinical requirements through clinical development, regulatory submission processes and post-approval / maintenance post-launch activities. Our experts use technology-elevated solutions to support clients through the entire product lifecycle.
View our content to discover how our expanded capabilities can help you – or contact a Cencora PharmaLex expert today with any questions.
CONTACT INFORMATION
Cencora PharmaLex
1 W 1st Ave.
Conshohocken, PA 19428
UNITED STATES
GET MORE DETAILS ON OUR SOLUTIONS
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Explore the top 3 insights on the impact of pre-approval communication and learn why healthcare decision makers want more pre-approval resources and engagement from manufacturers.
FEATURED INSIGHTS
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Understanding payer strategies for anti-obesity drugs is crucial. A recent study investigated commercial formulary trends, confirming cost as a major barrier despite positive patient outcomes.
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How are payers using value-based contracts for costly rare disease therapies? Exploratory research sheds light on negotiation frequency, preferred contract types, and internal data management trends.
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Research presented at AMCP 2025 uses natural language processing on decision-maker feedback to predict coverage. Learn about the surprising findings and next steps in this Q&A.
EXPLORE OUR THOUGHT LEADERSHIP
Explore the latest insights from the Cencora team.
WEBINARS
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Overview Of The UK's International Recognition Procedure
Gain clarity on the UK's International Recognition Procedure (IRP). Experts Chris Englerth and Graham Donaldson provide key insights into the process and its impact on pharmaceutical product approvals.
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Data Governance And AI In Pharma: Overcoming Challenges In DACH Region
Gain insights from industry experts on the implications of the EU's AI Act for data governance professionals, ensuring your organization remains compliant while leveraging AI's transformative potential.
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EU HTA – Achieving Broad Access Fast! What Will It Take For Innovative Medicines To Succeed?
Discover how to navigate the EU HTAR's Joint Clinical Assessment process. Learn from industry experts about accelerating patient access to innovative medicines in Europe.
WHITE PAPERS
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Why An Integrated Approach Ensures Smooth Entry Into The European Market
Simplify your EU launch and boost returns. Learn how to manage regulatory hurdles, access a huge patient population, and gain end-to-end commercial support.
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A CFO's Guide To Driving Growth
Navigate the evolving biotech landscape and secure venture capital with insights on strategic partnerships and investor expectations.
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20 Years Of Biosimilars: Are We On The Right Track?
Explore the transformative journey of biosimilars, 20 years in. Through industry expert insights collected from a recent panel discussion, explore regulatory hurdles, market shifts, and the path ahead.
PODCASTS
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Navigating The Digital Era And Beyond For Engaging Key Decision Makers In Specialty Pharmacy
Tune in as experts discuss how biopharma companies can effectively engage healthcare decision-makers in the evolving digital landscape.
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An Overview Of Contamination Control Strategy (CCS)
Join experts Londa Ritchey and Patrick Nieuwenhuizen as they explore the key role of a contamination control strategy in Annex 1 for ensuring patient safety and continuous manufacturing improvement.
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Assessing Gaps And Achieving Compliance With Annex 1
In this podcast episode on Annex 1 compliance and gap assessment, Patrick Nieuwenhuizen shares his insights and expertise gleaned from extensive experience in pharmaceutical regulation and compliance.