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API Intermediates & Impurities Services for Pharmaceutical Research
At Dr. KS Labs, we specialize in the synthesis of API intermediates and impurities, providing high-quality compounds to pharmaceutical companies for drug development, formulation, and quality control. Our services are designed to support regulatory requirements and ensure the highest standards of purity and safety in active pharmaceutical ingredients (APIs).
Key Services:
- API Intermediates: Synthesis of advanced intermediates required for the production of APIs, ensuring quality, consistency, and scalability.
- Impurity Standards: High-quality reference standards for impurities, compliant with USP, EP, and BP standards, to support pharmaceutical quality control and regulatory submissions.
- Process-Related Impurities: Design and synthesis of process-related impurities to ensure the safety and efficacy of drug substances during production and quality testing.
- Custom Synthesis of API Impurities: Tailored synthesis of API impurities that are not readily available commercially, helping accelerate research and development timelines.
- Impurity Identification & Control: Comprehensive impurity profiling, ensuring that all critical impurities are identified and controlled in line with regulatory requirements.
We offer a wide portfolio of API intermediates and impurities across therapeutic areas such as anti-cancer, anti-diabetic, anti-tuberculosis, anti-infective, anti-inflammatory, and more. With our deep expertise in organic synthesis and commitment to confidentiality, Dr. KS Labs delivers high-quality solutions for pharmaceutical research, ensuring that clients can meet their development goals efficiently and safely.