Our Services
Comprehensive Pharmaceutical Services
From formulation to finished goods, Ashford delivers end-to-end contract manufacturing capabilities under strict cGMP and FDA compliance.
Toll / Contract Manufacturing
Full-cycle manufacturing of sterile and non-sterile pharmaceuticals under cGMP and FDA compliance. Our flexible lines and experienced teams scale from pilot batches to commercial volumes.
- Sterile ophthalmic & otic solutions and ointments
- Non-sterile tablets, film-coated tablets, and capsules
- Creams and ointments
- Primary and secondary packaging
Repacking & Packaging Services
Comprehensive primary and secondary packaging — blistering, bottling, and labeling — across a wide range of dosage forms with full batch traceability.
- Ophthalmic & otic preparations
- Oral solids: tablets and capsules
- Semi-solids: creams and ointments
- Blistering, bottling, and labeling
Product Development
Our Technical Services team supports the full development lifecycle — from formulation to commercial production — backed by analytical and stability capabilities.
- Formulation development
- Scale-up and technology transfer
- Stability studies
- Commercialization support
Certificate of Listing of Identical Drug Product (CLIDP)
Regulatory support for listing identical drug products to streamline FDA registration. We help partners navigate documentation and compliance requirements with confidence.
- CLIDP application assistance
- Documentation and dossier support
- FDA registration guidance
- Ongoing compliance maintenance
Internship & Work Immersion
A structured program giving undergraduate students hands-on experience in a cGMP-compliant environment, mentored by qualified professionals across our operations.
- Real industry experience
- Exposure to cGMP operations
- Mentorship from professionals
- Pathway to future opportunities
A clear path from inquiry to delivery
- 1
Inquiry
We learn about your product, volumes, and timelines.
- 2
Feasibility
Technical and regulatory feasibility assessment.
- 3
Development
Formulation, scale-up, and technology transfer.
- 4
Regulatory
Documentation and FDA compliance support.
- 5
Manufacturing
cGMP production with full quality control.
- 6
Delivery
Quality-released finished goods, on schedule.
Let's Build a Healthier Future Together
Partner with Ashford for quality contract manufacturing.