With a thorough understanding of quality and fully comprehensive capabilities, BioStem Life Sciences is highly qualified to lead clients through the complex and fruitful process of bringing new and exciting products to market. From the very beginning, we can guide you through the infancy of your product development plans, all the way to final regulatory approval. Our team of skilled and seasoned project leaders will work closely with you to develop a product plan that meets your needs. Utilizing our expertise in both process development and quality, we can translate your idea or benchtop process into a fully scalable manufacturing process.
With a broad range of experience in product development and clinical production, BioStem has the insight and expertise to identify and address key issues as we work with you to produce your material. BioStem also offers full support for your IND filing by providing QA audited batch records for your Investigational New Drug (IND) filing including Chemistry, Manufacturing, and Control (CMC) support.
At BioStem Life Sciences, quality is essential to us because we value our customers' reputations and, above all else, their patients' safety. In our FDA registered, cGMP compliant lab, we strive to provide products and services which not only meet but exceed, Current Good Tissue Practice requirements.
If you have questions about the company, our lab, our scientific team or anything else, please feel free to contact us.Contact Us