Founded in Indianapolis in 2014, Genezen is focused on supporting the demands of the current and future gene and cell therapy manufacturing market worldwide— making viral vector production accessible to both early-stage, growth-oriented companies and established industry leaders. Genezen offers early-phase process development, GMP lentiviral vector production, retroviral vector production, and analytical testing services, building on the company's expansive knowledge and experience in the industry and working with the nation's leading institutions. For more information, or to learn more about services offered in Genezen's new cGMP facility, please visit our website: www.genezen.com
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1-10 employees
View all Genezen Laboratories employees
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Biotechnology
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9900 Westpoint Dr, Indianapolis, Indiana 46256, US
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2014
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Cgmp Manufacturing, Process Development, Assay Development, Cell Banking, Lentiviral Vector, Retroviral Vector, Viral Vector Manufacturing, Viral Vector Testing
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The decision makers in Genezen are Bill Vincent, Brok Weichbrodt, Hsiaolin Chang, etc. Click to Find Genezen decision makers emails.
You can reach Genezen Laboratories by visiting their website at http://genezen.com and using the contact form provided. Alternatively, you can call their main office directly or send an email to their support team for specific inquiries regarding services and solutions.
Yes, Genezen provides a staff directory on their website, showcasing key team members and their roles. This resource is helpful for understanding the expertise available and for reaching out to specific individuals regarding your project needs or inquiries.
Genezen supports a variety of industries, primarily focusing on gene and cell therapy sectors. Their expertise in viral vector manufacturing caters to both early-stage biotech companies and established pharmaceutical firms looking to advance their therapeutic solutions.
Genezen specializes in the production of lentiviral and retroviral vectors. Their cGMP manufacturing capabilities ensure that these vectors meet the rigorous standards required for clinical applications, making them suitable for a range of gene therapy projects.
Genezen adheres to cGMP (current Good Manufacturing Practices) standards throughout their manufacturing processes. This commitment to quality control ensures that all products meet regulatory requirements and maintain the highest standards for safety and efficacy in gene therapy applications.
Yes, Genezen encourages potential clients to schedule consultations with their team. You can request a meeting through their website's contact form, where you can specify your project needs and the relevant services you are interested in discussing.
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