by Jeffrey Wotton | May 30, 2025 | Biopharma Consultant, Biotech Consulting, GMP Good Manufacturing Practices, Insights, Pharma Consulting, Quality assurance compliance consulting
How to Prepare for a GMP Inspection: A Consultant’s Perspective Good Manufacturing Practice (GMP) inspections are pivotal events for pharmaceutical and biotech companies. A successful inspection can affirm your organization’s commitment to quality and regulatory...
by Jeffrey Wotton | Apr 4, 2025 | Biopharma Consultant, Insights, Pharma Consulting, Quality assurance compliance consulting
Leveraging a Biopharma Consultant for Regulatory Filing Readiness In the fast-paced world of pharmaceutical and biotechnology development, successfully navigating the regulatory landscape is a critical step toward bringing a product to market. From IND...
by Jeffrey Wotton | Apr 1, 2025 | Insights, Pharma Consulting, Quality assurance compliance consulting, Working Reference Standard, Working standard qualification
Understanding the Difference Between Working Standards and Reference Standards in Biopharma In the biopharmaceutical industry, accurate and consistent analytical testing is essential to ensure product quality, safety, and regulatory compliance. One of the key...
