Sourav Kundu
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Sourav Kundu is the director of process engineering in the process development department at Amgen, Inc.
Articles by Sourav Kundu
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- Biopharmaceutical Analysis
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- Biopharmaceutical Analysis: GC-MS
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- Biopharmaceutical Analysis: NMR
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- Deals, Development and Manufacturing
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- Excipients
- API Synthesis and Manufacturing, Large Molecule
- Formulation and Drug Delivery, Combination Drugs
- Early Phase Development
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- Discovery Pipeline
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- Manufacturing, Monoclonal Antibodies
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- Supply Chain/Logistics
- Manufacturing Best Practices
- Information Technology
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- Manufacturing Equipment, Upstream Processing
- Manufacturing Equipment, Biologics
- Cleanroom Equipment and Supplies
- Manufacturing, Parenterals and Injectables
- Clinical Trial Materials
- Manufacturing, Biosimilars and Biobetters
- Manufacturing, Lyophilization
- Manufacturing, Combination Drugs
- Manufacturing, Solid Dosage Drugs
- Manufacturing, Topical Drugs
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- Manufacturing, Nucleic Acids
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- Manufacturing, Drug Products
- Manufacturing, Cell Therapies
- Manufacturing, Recombinant Proteins
- Manufacturing, Continuous Biologics Processing
- Manufacturing, Gene Therapies
- Packaging, Labeling, and Distribution Systems
- Outsourcing
- Clinical Trial Services
- Perspectives on Outsourcing
- Contract Services, Regulatory Consulting
- Contract Packaging, Logistics, and Distribution
- Contract Manufacturing, Sterile, Aseptic Processing
- Contract Manufacturing, Biopharmaceutical Production
- Contract Manufacturing, Drug Substance, API
- Contract Manufacturing, Finished Drug Product
- Contract Manufacturing, General
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- Peer-Reviewed Research
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- Quality by Design
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- Standard Operating Procedures (SOPs)
- Quality Control/Quality Assurance
- Regulatory Filings and Submissions
- Regulatory Authority Actions
- Therapeutic Specific Areas
- Upstream Processing
- Viewpoints
- Weighing Up Big Pharma