Demonstrating experience, efficiency and technical proficiency in the development / validation of analytical methodology and GMP testing support.

Analytical Method Development and Validation
Small Molecule Evaluation
Stability-Indicating Assays
Stability Storage and Testing (On-Site ICH Testing)
Incoming Raw Material Testing and Release (On-Site GMP Testing)
Finished Product Testing and Release (On-Site GMP Testing)
Our 325,000ft² facility can manufacture up to 3 billion units. We supply oral pharmaceuticals to the U.S. market using our expertise in controlled release granules, serialization, blister and bottle packaging, powder packaging in stick packs, fluid bed operations, solvent processing, DEA controlled substances, high potency active ingredients and nanoparticle milling.
Frontida is a contract development and manufacturing organization that works collaboratively with clients to bring products to the pharmaceutical market. We offer formulation, analytical method development and validation, process development, commercial manufacturing packaging and more.

We strive to improve the pharmaceutical and biotechnology industries by working with scientists who are dedicated to coming up with the best solutions for clients and patients. Our team is also extensively experienced in the development and manufacturing of oral dosage forms, including tablets and capsules.