GMP-compliant facilities ensure safe, scalable, and consistent production of tablets, syrups, and suspensions like MOXEEZ and GRETLY. At Faraday Formulations Pvt. Ltd., we adhere strictly to Good Manufacturing Practices (GMP) to uphold the highest standards of pharmaceutical manufacturing. GMP compliance is not just a regulatory requirement; it is the foundation of our commitment to product quality, patient safety, and operational excellence These include:
We promote and distribute our products across multiple regions, ensuring timely access and seamless support to healthcare professionals and pharmacies. Our robust distribution network is strategically designed to cover urban, semi-urban, and rural areas, making essential medications readily available to those who need them most. By working closely with regional partners, logistics providers, and regulatory bodies, we maintain uninterrupted supply chains and meet the highest standards of compliance and safety.
Beyond product delivery, we also offer consistent medical support to doctors, pharmacists, and healthcare institutions. Our field teams provide up-to-date product information, therapeutic guidance, and real-time assistance to ensure optimal usage and patient outcomes
Through these integrated efforts, we not only ensure widespread availability of our products but also reinforce trust, reliability, and excellence in healthcare delivery across regions.
We offer comprehensive and customized solutions for our partner brands, tailoring services to meet their specific business and therapeutic needs. Our private labeling services allow clients to launch their own branded products without investing in large-scale manufacturing infrastructure. From concept development to packaging design and regulatory compliance, we manage the complete lifecycle to ensure quality, speed, and confidentiality.
In addition to branding, we specialize in developing therapeutic-specific formulations based on market demand, clinical relevance, and partner preferences.
Our agile manufacturing setup supports both small and large batch productions, making it ideal for pilot projects or mass-market launches. By integrating innovation, quality assurance, and market insight, we help our partners expand their portfolio, enter new markets faster, and meet the evolving needs of healthcare providers and patients.
Stringent quality assurance systems and robust regulatory support are fundamental to ensuring that every product we manufacture consistently meets the highest safety and efficacy benchmarks. At each stage of production—starting from the procurement of raw materials to the final packaging—our processes are guided by internationally recognized Good Manufacturing Practices (GMP).
Our dedicated quality control teams conduct rigorous testing to verify purity, stability, and therapeutic effectiveness. In addition, we continuously monitor and validate our procedures to adapt to evolving regulatory requirements and scientific advancements. This proactive approach minimizes risk and fosters confidence among healthcare providers and end users alike.