Biologic pharmaceuticals are more popular than ever, and with increasing sponsor demand and project complexity, CDMOs face mounting pressure to stand out in a crowded marketplace.
ISR’s Biologic Drug Product CDMO Benchmarking report reveals how sponsors evaluate providers, what they value, and which CDMOs deliver against expectations. Performance benchmarks and in-depth CDMO profiles highlight where an organization excels, where peers outperform, and opportunities to position strengths more effectively.
What you will learn:
Outsourcing Practices
- Proportion of manufacturing activities outsourced
- Main driver in outsourcing
- Preferred provider usage and management
CDMO Selection Drivers
- Top CDMO selection attributes
- Attributes growing in importance
CDMO Perceptions & Interactions
- CDMO brand familiarity and usage
- Leadership, preference, and proposal volume
- CDMO cost perceptions
CDMO Performance & Competitive Landscape
- How CDMOs measure up to sponsor expectations
- Competitive position across providers
Company Service Quality Profiles
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20+ CDMO profiles
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Customer feedback on 24 performance metrics
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Overall Satisfaction, Likelihood to Use Again, and Willingness to Recommend
Included Providers:
Companies listed in bold print have a Company Service Quality Profile page detailing company performance based on user ratings (currently using or have used in the past 18 months).
- AbbVie Contract Manufacturing
- Alcami
- Avid Bioservices
- Biovian
- Boehringer Ingelheim BioXcellence
- Bora
- Carbogen Amcis
- Catalent
- Celonic
- Cenexi
- CordenPharma
- Curia
- Enzene
- Famar
- Fareva
- Fujifilm Biotechnologies
- GSK Contract Manufacturing
- Hetero
- IDT Biologika
- Lonza
- MilliporeSigma, including BioReliance
- Next Pharma
- Novartis CDMO (Global Biotech Cooperations)
- Pace Analytical
- Patheon, by ThermoFisher Scientific
- PCI Pharma Services, including Ajinomoto Bio-Pharma Services
- Pfizer CentreOne
- Piramal Pharma Solutions
- Polpharma
- Pyramid Labs
- Recipharm
- Resilience
- Samsung Biologics
- Sandoz
- Siegfried
- Simtra
- Vetter
- Wockhardt
- WuXi Biologics
Respondents were required to pass several screening criteria to qualify and participate in this survey:
- Must work at a biopharmaceutical company
- Must have responsibilities in at least one of the following categories: executive management, R&D management, clinical operations, clinical trial manufacturing, commercial manufacturing, outsourcing/purchasing management, QA/QC, supply chain or validation
- Must have been involved in outsourced biologic drug product manufacturing within the past 18 months




