The Azopharma Inc

Industry:	Medical Testing & Clinical Laboratories
Revenues:	$2.7 Million
Employees:	51

Description

Azopharma specializes in drug development support for the pharmaceutical industry. We are experts at formulations, custom synthesis, isolation/purification, elucidation, characterization, method development and validation, clinical supplies for Phase I.

Azopharma supports product development for:


Drug substances and excipients
Oral dosages (tablets, capsules)
Topical dosages (creams, ointments, lotions)
Liquids dosages (injectables, suspensions)
Inhalation dosages (MDI, DPI, Nasal)
Biotech products
Nutraceuticals
Medical devices


We can perform cGMP compliant analyses using a variety of analytical techniques including FT-IR, NMR, SEM/EDXA, DSC, GC, HPLC and Direct Probe MS. We are also capable of combining these tools with proprietary polymer and physical testing methodologies to provide novel approaches to product release testing, package suitability and stability monitoring studies.

Azopharma is FDA registered and audited, DEA licensed and cGMP compliant. We welcome visits to our facility for audits or to outline a study that meets your specific needs.