Contract Manufacturer
As a contract manufacturer, N Lexo Pharma specializes in providing comprehensive manufacturing solutions tailored to the unique needs of our partners in the pharmaceutical industry. Our state-of-the-art facilities and advanced technologies enable us to produce a wide range of pharmaceutical products, ensuring compliance with stringent quality and regulatory standards.
We offer flexibility and scalability in our manufacturing processes, allowing our clients to focus on their core competencies while we handle the production of their products. Our team of experts collaborates closely with clients throughout the entire manufacturing cycle, from product development and formulation to packaging and distribution.
By leveraging our expertise and resources, we help our partners reduce costs, minimize time-to-market, and enhance their product offerings. Our commitment to quality assurance ensures that every product we manufacture meets the highest standards of safety and efficacy, reinforcing trust and reliability in the brands we support.
Through our contract manufacturing services, N Lexo Pharma is dedicated to fostering long-term partnerships that drive innovation and success within the pharmaceutical industry.
cGMP & GLP Compliance
At N Lexo Pharma, we go beyond compliance with the World Health Organization’s Good Manufacturing Practice (cGMP) and Good Laboratory Practice (GLP) standards. Our state-of-the-art quality control laboratories are equipped with advanced instruments to conduct thorough analysis of finished products, raw materials, and packaging materials, ensuring the highest standards of quality and safety. As a reputable manufacturer, we are also proud to be part of the Pharmaceutical Inspection Co-operation Scheme (PIC/S), reinforcing our commitment to maintaining globally recognized best practices in the pharmaceutical industry.
Contract Manufacturing with GLP Standards
At N Lexo Pharma, we ensure that all products manufactured under our contract manufacturing services undergo rigorous testing in accordance with Good Laboratory Practice (GLP) standards. This commitment guarantees that every product meets the highest quality, safety, and efficacy requirements. Our well-equipped laboratories and adherence to GLP guidelines enable us to conduct comprehensive testing and validation, covering everything from raw materials to finished products. By partnering with us, you can trust that your products will be manufactured and tested with precision and care, upholding global pharmaceutical quality standards.
Safety & Quality
Ensuring the safety and quality of medicines is a top priority for N Lexo Pharma, as we understand its importance to patients and healthcare providers alike. We are committed to maintaining the highest standards with a strict no-compromise policy on quality. Our quality system is continuously refined and enhanced, focusing on every aspect of quality management.
Since our establishment, N Lexo Pharma has successfully undergone over 100 inspections and audits by various health authorities around the world. These include the National Pharmaceutical Regulatory Agency (NPRA), the U.S. Food and Drug Administration (US FDA), and the Health Sciences Authority of Singapore, among others. This consistent approval demonstrates our unwavering dedication to quality and regulatory compliance, ensuring that our products meet global safety and efficacy standards.