The need for improved analytics grows.
Courtney LeBlon
Advertisement
Courtney LeBlon, PhD, is the director of technical operations for Ori Biotech.
Articles by Courtney LeBlon
Advertisement
Latest Updated Articles
Advertisement
Advertisement
- News
- Multimedia
- Publication
- Conferences
- Resources
- Subscribe
- Webcasts
- BioBusiness
- BioPharm Products
- BioPharm Sponsored Ad
- Biopharmaceutical Analysis
- Analytical Best Practices
- Analytical Methods
- Lab Furnishings and Equipment
- Contract Analytical Services
- Finished Product Analysis
- Drug Substance Analysis
- 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
- Biosimilars and Biobetters
- Deals, Development and Manufacturing
- Development
- Formulation
- Process Validation
- Drug Delivery
- Process Development
- Scale Up
- Excipients
- API Synthesis and Manufacturing, Large Molecule
- Formulation and Drug Delivery, Combination Drugs
- Early Phase Development
- Formulation and Drug Delivery, Biologic Drugs
- Formulation and Drug Delivery, Parenterals
- Formulation and Drug Delivery, Specialty Dosage Forms
- Formulation and Drug Delivery, Controlled Release
- Formulation and Drug Delivery, Liquids
- Formulation and Drug Delivery, Solid Dosage
- Formulation and Drug Delivery, Other
- Discovery Pipeline
- Disposables Advisor
- Downstream Processing
- Elements of Biopharmaceutical Production
- From the CEO
- From the Editor
- Inside Standards
- Interphex Keynote Sessions
- Manufacturing
- Manufacturing, Monoclonal Antibodies
- Manufacturing Systems, Single-Use
- Vaccine Development and Manufacturing
- Manufacturing, Aseptic Processing
- Manufacturing, Fill/Finish
- Facility Design and Engineering
- Process Control, Automation, and PAT
- Supply Chain/Logistics
- Manufacturing Best Practices
- Information Technology
- Technology Transfer
- 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
- Manufacturing, Biologics
- 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
- Contract Services, Formulation and Drug Delivery
- Peer-Reviewed Research
- Pharmacopoeial Compliance Series
- Quality/GMPs
- Ask the Expert
- Regulatory/GMP Compliance
- Compliance Notes
- Regulatory Beat
- European Regulatory Watch
- Adverse Events and Recalls
- Regulatory/GMP Compliance, Europe
- Regulatory/GMP Compliance, Emerging Markets
- Audits and Inspections
- Anticounterfeiting, Track and Trace Systems
- Quality by Design
- Compendial Compliance
- 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
