Salem, NH

Drug development services from this site advance candidates from early pre-formulation and tox studies to an IND filing and on through the clinical phases. Our GMP clinical supplies manufacturing capabilities include sterile fill-finish and clinical packaging and kitting. Our teams have proven expertise with small molecules, biologics (such as proteins, peptides, antibodies, antibody drug conjugates) and gene therapies (such as RNA and DNA oligos).

• Contract Development Manufacturing Organization (CDMO)
• 30,000 ft² GMP Clinical Manufacturing Facility
• Providing Services for More Than 30 years

Core Services:

• Formulation Development
• Process Development
• Full Analytical Support
• Aseptic Manufacturing: Ophthalmic, Otic, and Injectable Products
• Toxicology Enabling Materials
• Phase 1 / Phase 2 Clinical Trial Materials
• Niche Commercial Manufacturing
• Batch Sizes:
  • Automated Fills – Ophthalmics from 100’s Of Units up to ~50,000 Units Per Batch
    • Manual Fills – Injectables up to 2,500 Units/Batch
    • Small Minimum Batch Sizes, 100 ml to 100 liters