Synfine Drugs Private Limited | Synfine Drugs Private Limited

Since our inception in 2020, we have consistently excelled as a reputable manufacturer and exporter of a wide range of Active Pharmaceutical Ingredients (APIs) and Intermediates. Our commitment to unwavering quality and strict compliance is evident through our ISO 9001:2015 certification and steadfast adherence to Good Manufacturing Practices (GMP) standards.

We take immense pride in our capacity to support our regulatory-focused customers by offering comprehensive documentation essential for Drug Master File (DMF) submissions. Recognizing the pivotal role of regulatory compliance in the pharmaceutical industry, we are devoted to guiding our clients through the intricate regulatory landscape.

Our dedication to excellence extends to our commitment to expand our product portfolio, explore new opportunities, and bolster partnerships within the pharmaceutical sector. We consistently invest in research and development to remain at the forefront of technological advancements, ensuring our customers receive cutting-edge products and services.

Synfine Drugs’ steadfast commitment to quality, compliance, affordability, and customer satisfaction establishes us as a trusted partner for pharmaceutical manufacturers worldwide. We are eager to seize the opportunity to meet your pharmaceutical needs and contribute to advancing global healthcare through our exceptional APIs and intermediates.