AMF Pharma
Contract manufacturer of over‑the‑counter (OTC) pharmaceutical products offering licensed cGMP manufacturing, turnkey private‑label services, formulation development, packaging and labeling, and regulatory/quality support. Facilities are certified and registered with relevant US authorities; minimum order quantities and lead times are provided for production planning.
Industries
Nr. of Employees
small (1-50)
AMF Pharma
Ontario, California, United States, North America
Services
End‑to‑end contract manufacturing services for OTC products, including formulation, production, packaging, and labeling for private‑label and custom projects.
R&D services to develop and optimize OTC formulations across multiple dosage forms and support scale-up to commercial production.
Packaging operations and label design integrated with manufacturing to deliver finished OTC products ready for market.
Implementation of quality systems, internal audits, training, and support for regulatory inspections and facility registrations.
End‑to‑end contract manufacturing services for OTC products, including formulation, production, packaging, and labeling for private‑label and custom projects.
R&D services to develop and optimize OTC formulations across multiple dosage forms and support scale-up to commercial production.
Packaging operations and label design integrated with manufacturing to deliver finished OTC products ready for market.
Implementation of quality systems, internal audits, training, and support for regulatory inspections and facility registrations.
Expertise Areas
- OTC drug contract manufacturing
- Formulation development and scale-up
- Private label manufacturing
- cGMP compliance and quality management
Key Technologies
- cGMP manufacturing processes
- Formulation development for tablets, capsules, liquids, softgels, and topical products
- Scale-up and batch-size flexibility
- Packaging and label design workflows
News & Updates
Processes and systems certified as compliant with cGMP standards by a third‑party registrar.
Facility registered as a manufacturer with the California Department of Public Health.
Production facilities reported to meet or exceed applicable US FDA criteria and prepared for regulatory inspection.
Processes and systems certified as compliant with cGMP standards by a third‑party registrar.
Facility registered as a manufacturer with the California Department of Public Health.
Production facilities reported to meet or exceed applicable US FDA criteria and prepared for regulatory inspection.