Mayne Pharma Group Limited (Mayne Pharma) is an ASX-listed specialty pharmaceutical company focused on applying its drug delivery expertise to commercialize branded and generic pharmaceuticals. Mayne Pharma also provides contract development and manufacturing services to more than 100 clients worldwide.
Mayne Pharma's roots can be traced to FH Faulding and Co, for many years one of the largest and most prominent public companies headquartered in South Australia.
A technology driven company, Mayne Pharma has a significant product portfolio and pipeline, global reach through distribution partners in Australia, North America, Europe and Asia and two product development and manufacturing facilities based in Salisbury, Australia and Greenville, North Carolina, USA with expertise in formulating complex oral dose forms including highly potent compounds, controlled substances, modified release products and inherently unstable compounds. The business is supported by over 850 staff globally with more than 200 scientists employed.
The 12,000m2 facility in Salisbury, South Australia is capable of developing products from formulation and clinical trial stages to validation and registration, right through to commercial scale manufacture of packaged goods. The Salisbury site:
Is GMP compliant as certified by chief regulatory authorities (FDA, TGA and with mutual recognition from the MHRA, TPD and various Asian regulatory authorities).
Is licensed to handle CII/S8 compounds (controlled drug substances) and utilize chlorinated solvents and alcohols in the manufacturing process.
Includes an established manufacturing facility with capacity to produce 2.5 billion capsules and tablets, 100 ton of bulk product and 16 million units of liquid and cream product annually.
Includes extensive product development laboratory space to accommodate all analytical processes and bench scale formulation through to pilot scale manufacturing and scale-up for multiple concurrent development projects.
Is a center for product development activities, from formulation and clinical trial stage, to validation and registration, to commercial scale manufacture of packaged goods ready to be dispensed.
The 11,700m2 facility in Greenville, North Carolina specializes in complex dosage forms including potent compounds, Schedule II-V controlled substances, inherently unstable compounds and products with poor bioequivalence. The Greenville site:
Offers quality pharmaceutical formulation development, analytical testing services and commercial and Phase I, II and III Clinical Trial Manufacturing (CTM).
Offers particular expertise in First-Time-In-Man (FTIM) and Phase I, II, and III CTM - conducting more than 140 FTIM projects for different chemical entities while concurrently developing more than 700 CTM batches.
Is GMP compliant as certified by chief regulatory authorities (FDA and MHRA).
Includes an established manufacturing facility with capacity to produce over 1.0 billion tablets and capsules annually.
Is capable of handling potent products and is DEA-approved for Schedule II-V controlled substances.