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- Importance of Preformulation Studies In Drug Development
- Understanding Current Good Manufacturing Practice Regulations: A Comprehensive Guide to Compliance
- The Strategic Advantage of Partnering With Mid-Size Pharma Companies
- Prescription for Success: Primary Packaging vs. Secondary Packaging in Pharmaceuticals
- Small Molecule Drug Development
- Pharmaceutical Serialization and Aggregation DSCSA Compliance
- Microbiological Testing Lab Services
- Drug Delivery Dynamics: A Closer Look at Extended Release vs. Sustained Release Tablets
- IND, NDA & ANDA Challenges and How a CDMO Can Help
- ICH Stability: A Guide to ICH Stability Storage and Testing for Pharmaceuticals
- Highly Potent API Development: Strategies, Safety Protocols, and Best Practices
- Clinical Trial Material Manufacturing: What Is CTM?
- UPM Drug Product Manufacturing Solutions & Processes
- What Is a CDMO?
- 5 Key Objectives of Quality Assurance in the Pharmaceutical Industry
- Why Is Pharmaceutical Quality Assurance Important?
- Fluid-Bed Granulation in Pharmaceutical Manufacturing
- DEA-Approved Vault Space Guidelines
- The Orphan Drug Designation - Benefits of Orphan Drug Exclusivity and Its Use During the COVID-19 Pandemic
- The Drug Development Process with UPM Pharmaceuticals
- Over the Counter Contract Manufacturing with UPM Pharmaceuticals
- Our Capabilities as a Generic Drug Manufacturer
- Semi-Solid & OTC Topical Manufacturing
- Critical Aspects of the Dry Blending
- Why Outsourcing to Oral Solid Dosage Manufacturing Companies Is the Smart Choice for Innovators
- Generic Drug Manufacturer Trends: Reshoring From Overseas Back to the US Market
- How to Choose the Right Pharmaceutical Contract Manufacturer
- Clinical Trial Supply Management: The Importance of the Clinical Batch Manufacturing Supply Chain
- Pharma Tech Transfer Best Practices