Best Pharmaceutical Laboratories In Melbourne Near Me

4worldlovers:

Risk to Resilience: a rood map to vaccine access for older Australians

We make innovative vaccines and specialty medicines to prevent and treat disease. Our R&D focuses on the science of the immune system, human genetics and advanced technologies.

4worldlovers: Our state-of-the-art manufacturing facilities are TGA approved as well as being USFDA (USA) and MHRA (UK) approved. Cipla Australia has over 200 registered formulations with TGA through partnerships with market leaders and on its own. The list of registered medicines includes OTC (Over the Counter), Prescription and hospital medicines. We are also involved in helping Australians access medicines through the SAS (Special Access Scheme). Cipla has earned a name for maintaining world-class quality across all our manufacturing units, products and services. Globally, our patent filing includes drug substances, drug products, platform technologies, IP on polymorphs and crystallinity, and medical devices.

4worldlovers:
We offer a comprehensive solution for global sample sourcing, catering to the needs of pharmaceutical companies and clinical research organizations. Our services encompass both single and multiple batch drugs, ensuring streamlined processes and convenience for our clients. Pro Pharmaceuticals Group holds wholesaler licenses issued by the Victorian Department of Health, including authorization for the handling of controlled drugs. Our commitment to compliance and quality is reflected in our robust infrastructure and storage facilities.

We maintain licensed wholesaler storage sites strategically located in Tullamarine, Melbourne, and Cheltenham, Melbourne. These sites adhere to stringent temperature and humidity controls, aligning with ISO 9000 standards and Good Distribution Practices (GDP). By prioritizing optimal storage conditions, we uphold the integrity and stability of the products we handle.

Furthermore, we have a licensed EU GMP manufacturing site in Warsaw, Poland. This facility operates in accordance with European Union Good Manufacturing Practices (EU GMP) standards. Our capabilities at this site include EU GMP repacking, Qualified Person (QP) release, and distribution of clinical trial supplies within Europe or other global regions. Additionally, we offer secondary labeling services (under GMP) to meet the specific requirements for supplying to Australia.