Naveen Pathak
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Naveen Pathak is a principal engineer in the process development department at Amgen, Inc.
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- Biopharmaceutical Analysis
- Analytical Best Practices
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- Biopharmaceutical Analysis: GC-MS
- Biopharmaceutical Analysis: Mass Spectrometry
- Biopharmaceutical Analysis: ICP-MS
- Biopharmaceutical Analysis: NMR
- Biopharmaceutical Analysis: Raman
- Biopharmaceutical Analysis: Gas Chromatography
- Biopharmaceutical Analysis: LC-MS
- Biopharmaceutical Analysis: HPLC/UHPLC
- Analytical Instrumentation
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- Deals, Development and Manufacturing
- Development
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- Process Development
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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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- Interphex Keynote Sessions
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- Manufacturing, Monoclonal Antibodies
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- Facility Design and Engineering
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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, Specialty Dosage Forms
- Manufacturing, Nucleic Acids
- Manufacturing, Liquid Drug Products
- 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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- Quality by Design
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- Standard Operating Procedures (SOPs)
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- Regulatory Filings and Submissions
- Regulatory Authority Actions
- Therapeutic Specific Areas
- Upstream Processing
- Viewpoints
- Weighing Up Big Pharma