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ASHFORDPharmaceutical Laboratories, Inc.
Ashford Pharmaceutical Laboratories manufacturing plant building

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 at Ashford
Contract Manufacturing

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 and packaging line at Ashford
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 and formulation at Ashford
R&D

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 regulatory documentation and compliance
Regulatory

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
Hands-on experience in Ashford operations and warehousing
People

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
How We Work

A clear path from inquiry to delivery

  1. 1

    Inquiry

    We learn about your product, volumes, and timelines.

  2. 2

    Feasibility

    Technical and regulatory feasibility assessment.

  3. 3

    Development

    Formulation, scale-up, and technology transfer.

  4. 4

    Regulatory

    Documentation and FDA compliance support.

  5. 5

    Manufacturing

    cGMP production with full quality control.

  6. 6

    Delivery

    Quality-released finished goods, on schedule.

Let's Build a Healthier Future Together

Partner with Ashford for quality contract manufacturing.