De Novo Peptide Sequencing by Tandem Mass Spectrometry: When It Is Needed and How It Works
Introduction De Novo Peptide Sequencing by Tandem Mass Spectrometry is a sophisticated analytical proteomics technique used to determine the precise […]
Cross-Border Drug Development: One Testing Lab for Both FDA and Health Canada Submissions
Generic Drug Development CDMO Cross-Border Drug Development: One Testing Lab for Both FDA and Health Canada Submissions By Anusha Sinha
What Is the Difference Between a Peptide and a Small-Molecule Drug in Manufacturing?
Peptide vs Small-Molecule CMC What Is the Difference Between a Peptide and a Small-Molecule Drug in Manufacturing? By Anusha Sinha
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United States vs. Overseas Peptide CDMOs: Should You Reshore Your Supply Chain?
Peptide CDMO Strategy United States vs. Overseas Peptide CDMOs: Should You Reshore Your Supply Chain? By Anusha Sinha • August
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Regulatory Pathway for Dexamethasone ANDA Submission
Introduction: A successful Dexamethasone ANDA Submission involves far more than demonstrating that a generic product contains the same active pharmaceutical
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What Is the Difference Between Biosimilarity and Interchangeability for Biosimilar Products?
Introduction The primary Difference Between Biosimilarity and Interchangeability lies in regulatory designation and pharmacy-level substitution rights rather than any variation
Case Study: Extractables and Leachables (E&L) Compliance for a Dry Powder Inhaler Seeking EMA Approval
Introduction Achieving Extractables and Leachables (E&L) Compliance for a Dry Powder Inhaler intended for European Medicines Agency (EMA) approval demands
Selectivity and Specificity in Bioanalytical Method Validation: What They Mean and How to Demonstrate Them
Bioanalytical Method Validation Selectivity and Specificity in Bioanalytical Method Validation: What They Mean and How to Demonstrate Them By Anusha