QSEM India’s Technology Transfer services ensure a smooth and efficient transition of pharmaceutical products from R&D to commercial manufacturing, maintaining quality, compliance, and scalability at every step.
We provide end-to-end support for transferring drug formulations, manufacturing processes, analytical methods, and ensuring reproducibility, scalability, and regulatory compliance. Our team of experts works closely with clients to optimize process parameters, conduct risk assessments, develop detailed batch manufacturing records, and validate analytical and manufacturing methods according to ICH, FDA, and EMA guidelines. By integrating robust quality systems, process characterization, and regulatory documentation, QSEM India minimizes technical and operational risks during scale-up. Our technology transfer services cover sterile and non-sterile formulations, small molecules, biologics, and complex dosage forms, enabling pharmaceutical and biotech companies to accelerate time-to-market while maintaining product safety, efficacy, and consistent quality.