We are an innovative CRDMO (Contract Research Development and Manufacturing Organization) located in Illinois, USA. We are a team of experienced industry experts with know how around chemistry development, supply material for toxicology studies, API manufacturing, technology transfer, NCE validations, Revalidations and commercial manufacturing.

Krystal biosciences offers a comprehensive portfolio of research, development, and scale up capabilities. We endeavor to meet the needs of pharmaceutical, biotechnology, consumer and material sciences industries to enable them to achieve their program milestones.

We envision to provide quality and transparency in our services for partners and to enable them conduct next phase of drug development activities. We strive for excellence in our chemistry through knowledge and hard work. We consistently improve our processes to bring better technologies that will help patient outcomes. We further pay utmost regard to our customers goals and act with speed and responsibility.

Dr. Siraj, is experienced in medicinal chemistry, chemical development, API Validations and drug delivery areas of Pharmaceuticals. He has strong understanding and competence in Chemical development, API chemistry design, validation’s and commercial manufacturing and Global Tech Transfers. His association with Cambridge Major Labs, Regis Technologies and Baxter Healthcare affords appropriate experience to your chemistry projects and is the purpose of Krystal Biosciences. Siraj earned his PhD in organic chemistry along with Post-doctoral work’s at Roswell Park cancer institute and Georgia Tech.

Lee brings breadth of experiences in areas of Quality assurance and regulatory compliance. He held leadership positions in quality and regulatory departments for global pharmaceutical and consumers companies. Lee brings GMP compliance management to organizations and develops robust SOP implementation programs. He is a valuable resource for Krystal Biosciences as Quality/Regulatory Advisor.