MANUFACTURING

•  At GOLD Pharma, we have invested in state-of-the-art infrastructure to ensure the highest quality standards. As a vertically integrated company, we manufacture our own early-stage intermediates, providing us with complete control over the production process and timely deliveries. We are dedicated to advancing green chemistry principles by embracing innovative processes and technologies. This commitment allows us to deliver significant advantages to our strategic partners who rely on us for their formulation needs. 

Our integrated Quality Control laboratory is equipped with state-of-the-art analytical instruments, adhering to the highest standards of quality assurance. We utilize advanced equipment, including HPLCs, GCs , HPLC systems, UV/VIS spectrophotometers, digital polarimeters for precise and comprehensive testing. Impurity profiling and product analysis are routinely conducted as an integral part of our stringent quality management protocols.

 As a global supplier in the pharmaceutical industry, we at GOLD PHARMA regard quality as fundamental to both our manufacturing processes and overall success. 

 GOLD Pharma boasts strong expertise in regulatory frameworks and a wealth of experience in regulatory filings. In addition to playing a vital role in ensuring full compliance with country- and region-specific regulatory requirements, our team excels in the preparation and compilation of DMFs and CTDs for submission to regulatory authorities worldwide, including the EU, Brazil, Canada, South Africa, Mexico, Turkey, Jordan, Iran, Taiwan, Indonesia, and more.

 Our regulatory team is continuously kept up-to-date on global regulatory standards, ensuring the accurate organization of data generation in line with submission guidelines mandated by relevant authorities.