Clive E. Badman, OBE, talks to CTA’s Charlie Abrines about the digitization of...
- Industry Viewpoints: Digitizing Clinical Manufacturing
- The Brexit Clock is Ticking, Are You Ready?
- Expert Insights: Serialization is a Necessary Step to Pharma Industry’s Adoption of Blockchain
- Considerations for Manufacturing Investigational Medicinal Products for Clinical Studies
- How to Maximize Randomization and Trial Management Systems in Clinical Studies
Industry Viewpoints: Digitizing Clinical Manufacturing
Clive E. Badman, OBE, talks to CTA’s Charlie Abrines about the digitization of the clinical supply chain
Early Phase Trials: Streamlining Your Biologics Process to Optimize Supply
Jonas Fransson, Director Drug Product Development, Swedish Orphan Biovitrum AB, shares the steps and activities to get your biological clinical trial material ready
Industry Viewpoints: Investigator-Initiated Studies – A Challenge for Supply with IMPs?
Peter Orosz, Head of Clinical Supply Chain Management & Oncology, Boehringer Ingelheim, addresses the challenges of investigator-initiated clinical trials
Serialization of Prescription Drugs: Readiness from Development into Commercialization
Hector Tamburini, Exec. Director, Regulatory Affairs & CMC, Prometheus Laboratories, examines how the industry needs to comply with regulations concerning serialization
The Million Dollar Question – How can Technology Improve Efficiency in the Clinical Supply Chain?
Rey Bacchus, Clinical Trial Supply Manager, Janssen Pharmaceutical R&D, examines what impact novel technology will have on supply chain processes
Expert Insights: Serialization is a Necessary Step to Pharma Industry’s Adoption of Blockchain
Peter Shapiro, Editor-In-Chief, PharmSource, guest writes for CTA and examines how serialization is key to a wider adoption of blockchain in pharma
Considerations for Manufacturing Investigational Medicinal Products for Clinical Studies
Kavita Vermani, Adamas Pharmaceuticals, Inc., explains the considerations required for the manufacture and release of investigational drug products
How to Maximize Randomization and Trial Management Systems in Clinical Studies
Francesco Spoto, Clinical Study Expert, highlights the advantages of using IRT solutions for pharma's SMEs and the best strategies to reap its benefits
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