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Development
Formulation
Analytical Services
Solubility & Bioavailability Enhancement
Micro and Nanotechnology
Drug / Device Combination Products
Biopharmaceutical
Proprietary Technology
Feasibility Programs
Manufacturing
Aseptic Manufacturing
Pre-clinical Manufacturing
Clinical Manufacturing
Commercial Manufacturing
Analytical Services
ICH – Stability Programs
Dosage Forms
Solutions and Suspensions Dosage Forms
Implantable Drug Delivery Systems and Combination Products Dosage Forms
Oral Solid Dose Dosage Forms
Semi-Solids and Gels Dosage Forms
Powders Dosage Forms
Markets
Ophthalmic CDMO
Long-Acting Drug Delivery CDMO
Oral Drug Delivery CDMO
Topical, Mucosal, and Transdermal CDMO
Injectables / Parenteral CDMO
Resources
Our Blog
Case Studies
Guides / White Papers
Brochures
Published Articles
Scientific Publications
Technical Briefs
Webinars / Podcast / Presentations
About Us
Employment
Events
Management Team
Press Releases
Contact Us
Our Blog
Featured Post
Guide to Inhalation and Respiratory Aerosol Drug Delivery: Leveraging CDMO Expertise
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Bridging Clinical and Commercial Drug Product Manufacturing – Outsourcing Advice from a CDMO
Ocular Implants for Drug Delivery: Improving Patient Outcomes
Nasal Drug Formulation: A Guide to Successful Drug Product Development
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2023 Pharma Trends Shaping the CDMO Industry Outlook
Phase Appropriate Filter Validation for Sterile Drug Product Manufacturing
Filter Validation: Key Elements for Sterile Drug Product Manufacturing
A 2023 Guide to Solubility Improvement and Bioavailability Enhancement Techniques
Excipient Selection and Supply for Complex Drug Products
Molecule to Market Podcast: The Value of Diversity in Pharma
A Pharmaceutical Guide to Cannabis – FAQs for Drug Product Development
A 2023 Guide to Vaccine Development & Immunization
The Guide to Analytical Method Development
Key Takeaways From the FDA Complex Generic Drug Product Development Workshop: Part 2
Key Takeaways From the FDA Complex Generic Drug Product Development Workshop: Part 1
How Personalized Medicine is Evolving the CDMO Landscape
Lyophilization of Pharmaceuticals: An Overview
Orphan Drug Product Development: Incentives and Outsourcing Considerations
Understanding Analytical Method Validation with Laurie Goldman
The FDA’s Recent Uptick in Ophthalmic NDA & BLA Approvals
Overcoming Solubility Challenges: Techniques to Improve Dissolution Rate and Increase Bioavailability
Highly Potent API (HPAPI) Handling: An Expert Interview with Judy Cohen
Aseptic Manufacturing and Sterile Fill-Finish for Complex Drug Products
6 Takeaways from the FDA’s Complex Generic Drug Product Development Workshop
Hot Melt Extrusion: Solubility Enhancement, Controlled Release, and More
Why the FDA Loves Complex Generic Drug Products
Nanomilling: A Key Option for Formulating Water-Insoluble APIs
What are Complex Drug Products and Why Should You Care?
