Product Development
Mayne Pharma has a proven track record in the development, optimisation and scale-up of generic and branded, innovative products for over the counter and prescription purchase. In addition we also provide value added active pharmaceutical ingredients (APIs) with off-patent drugs or new chemical entities (NCEs) for local and international markets.
Mayne Pharma offers product development options in conjunction with associated services, via its product development facility which is comprised of analytical laboratories and pilot scale production facilities that allow for a continuous scale up pathway from bench scale formulation to full commercial manufacture.
All facilities have been approved by international regulatory authorities including TGA, FDA, TPD and MHRA. Furthermore Mayne Pharma meets GMP and GLP standards for clinical supplies, thus accrediting our company to fulfill your requirements to ensure your products meet international standards. Mayne Pharma has experience shipping product, including clinical trial supplies, to any location in the world.
Download Clinical trial supplies and specialty services brochure (PDF)