
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 through to commercial production — backed by analytical and stability expertise.
- Formulation development
- Scale-up and technology transfer
- Stability studies
- Commercialization support

CLDP — Certificate of Listing of Identical Drug Product
Regulatory support for listing identical drug products to streamline FDA registration. We help partners navigate documentation and compliance requirements with confidence.
- CLDP 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.