About Us
AR Lifesciences is a renowned pharmaceutical manufacturing company that specializes in the production of high-quality generic tablets and capsules. As a WHO GMP Certified company, we adhere to strict international standards to ensure the safety, efficacy, and reliability of our medications. With a firm establishment in 2017, we have quickly emerged as a trusted name in the industry, driven by our vision to supply medicines at affordable prices without compromising on quality.
What We Do
At AR Lifesciences, we provide comprehensive contract manufacturing services to various esteemed brands within the pharmaceutical industry. Our state-of-the-art facility, combined with advanced technology and cutting-edge equipment, enables us to offer efficient and reliable solutions for the production of tablets and capsules. We work closely with our clients to understand their specific requirements and tailor our manufacturing processes to meet their unique needs. With a strong emphasis on quality control, we ensure that every product leaving our facility undergoes rigorous testing and inspection to uphold our commitment to excellence.
Our Commitment
At AR Lifesciences, our commitment to quality extends beyond manufacturing excellence. We are dedicated to ensuring that our clients have all the necessary support for regulatory compliance and successful product registration. By maintaining robust QA/QC practices and providing comprehensive documentation, including CTD dossiers and other required documents, we streamline the registration process for our clients. This commitment underscores our mission to not only manufacture high-quality medications but also contribute to the growth and success of our clients in the global pharmaceutical market.
In-House QA/QC and Document Management
At AR Lifesciences, we prioritize product quality and compliance with regulatory standards. To achieve this, we have a dedicated in-house Quality Assurance (QA) and Quality Control (QC) department. Our experienced and highly skilled QA/QC professionals oversee every step of the manufacturing process, from raw material sourcing to finished product inspection. Through meticulous testing and analysis, they ensure that our products meet the highest standards of quality, purity, and efficacy.
In addition, we maintain comprehensive documentation throughout the manufacturing process. We understand the importance of regulatory compliance and the need for accurate and complete documentation for registration purposes. Our team meticulously maintains all necessary documents, including the Common Technical Document (CTD) dossiers, to support the registration process in regulatory agencies. These documents contain critical information about the manufacturing process,
formulation, quality control, and safety profiles of our products. By providing comprehensive documentation, we facilitate the smooth registration of our clients' products in various regulatory markets.