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Andelyn Biosciences - CDMO/CMO
Andelyn Biosciences is a forward-thinking CDMO with a focus on gene therapy products. They offer a comprehensive suite of services including viral vector development, GMP manufacturing, and analytical testing. Their expertise in AAV and lentiviral vectors makes them a key partner for clients in the gene therapy space.
United States
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Specialized in gene therapy and viral vector production.
Expertise in both clinical and commercial scale manufacturing.
Focus on quality, safety, and regulatory excellence in biologics.
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Biologics
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Biologics
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Contact Andelyn Biosciences for Contract Services Expertise
Connect with Andelyn Biosciences, a leading pharmaceutical company from United States. They offer specialized CMO/CDMO - Contract (Development) Manufacturing Organizations, of which the services for CMO/CDMO include Gene and cell therapy products. Contact Andelyn Biosciences for free and discover if they are the perfect partner for your pharmaceutical needs.
CMO/CDMO - Contract (Development) Manufacturing Organizations
CDMOs and CMOs are pivotal in the pharmaceutical and biotech industries, offering specialized services in drug development and manufacturing. They assist in scaling up production from laboratory to commercial quantities, while adhering to strict regulatory standards. These organizations play a crucial role in the efficient and cost-effective production of medical and pharmaceutical products, ensuring quality and compliance at every stage.
Pharmaoffer's category for Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) encompasses a wide range of specialized services crucial to the pharmaceutical and biotech sectors. These organizations, often referred to as pharmaceutical CDMOs or drug CMOs, are instrumental in advancing drug development and manufacturing processes.
Key Functions of CMOs/CDMOs:
Drug Development and Manufacturing Expertise: Offering comprehensive services in drug development, from initial research and development to full-scale manufacturing. This includes CDMO services and CMO manufacturing, ensuring a seamless transition from concept to market.
Scalability Solutions: Assisting in scaling production from laboratory to commercial scale, meeting the demands of various projects while maintaining quality and efficiency. This is where the expertise of a full-service CDMO becomes invaluable.
Regulatory Compliance and Quality Assurance: Ensuring adherence to strict regulatory standards such as FDA and EMA guidelines, and implementing rigorous quality control measures throughout the manufacturing process. This includes operating within GMP certified facilities to guarantee the highest standards of production.
Cost-Effective Production: Providing efficient and cost-effective solutions for the production of medical and pharmaceutical products, enabling companies to focus on innovation and marketing. CMO contract manufacturing plays a key role in this aspect.
End-to-End Service Provision: From concept to commercialization, CMOs/CDMOs offer a range of services including process optimization, formulation development, clinical trial material production, and commercial manufacturing. This comprehensive approach is often referred to as Contract Development Manufacturing.
Connect with Leading CMOs/CDMOs
Through Pharmaoffer, you can explore and connect with a comprehensive range of CMOs/CDMOs. Our platform offers access to organizations that play a vital role in the efficient, quality-assured, and compliant production of pharmaceutical and medical products, supporting the industry's growth and innovation. Whether you're looking for a CDMO partner, CDMO solutions, or contract manufacturers in pharma, Pharmaoffer is your gateway to the best in the industry.
Biologics
Biologics CMOs/CDMOs specialize in the manufacturing and development of biopharmaceutical products, which are typically derived from living organisms or biological sources such as proteins, antibodies, vaccines, and cell therapies.
Biologics Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) encompass specialists in the production and development of biopharmaceuticals. These products, often derived from living organisms or biological sources, include proteins, antibodies, vaccines, and cell therapies. This sector includes biologics manufacturers, biopharma CDMOs, and companies dedicated to biologics development and biologic drug manufacturing.
Key Services Provided by Our Listed Biologics CMOs/CDMOs:
Advanced Biopharmaceutical Manufacturing: Utilization of cutting-edge biomanufacturing processes for the production of biologics, ensuring high purity, efficacy, and safety. This includes comprehensive biologics manufacturing and contract manufacturing biologics services.
Custom Antibody and Protein Development: Expertise in developing a range of biologic products, including monoclonal antibodies and therapeutic proteins, tailored to specific therapeutic needs. This is a key focus for many biologics companies and CDMO biotech firms.
Vaccine Production: Specialization in the manufacturing of vaccines using advanced technologies, contributing to global health and disease prevention efforts. This is a critical service offered by CMO biologics and biologics CDMO list members.
Cell Therapy Development: Capability to develop and manufacture innovative cell therapies, offering new treatment possibilities in regenerative medicine and oncology. This is a rapidly growing area within biologics development.
Regulatory Expertise: In-depth knowledge of the regulatory environment governing biologics, ensuring compliance with standards set by agencies like the FDA and EMA. This expertise is vital for all aspects of biopharmaceutical manufacturing.
Your Partner in Biologics Development and Manufacturing
Pharmaoffer provides a platform to connect with CMOs/CDMOs specializing in biologics. Our category ensures easy access to organizations that are equipped with the expertise and technology required for the complex development and manufacturing processes of biopharmaceutical products.
Gene and cell therapy products
Gene and cell therapy products are at the forefront of personalized medicine, treating genetic and acquired diseases. Their production involves advanced techniques to modify genes or cells, requiring stringent safety and efficacy standards, revolutionizing treatment paradigms.
At Pharmaoffer, we feature Contract Development and Manufacturing Organizations (CDMOs) that are pioneers in the field of gene and cell therapy products. These innovative therapies represent a significant advancement in personalized medicine, offering targeted treatments for genetic and acquired diseases. This includes expertise in Gene and Cell Therapy Drug Manufacturing and Gene and Cell Therapy Production.
Key Services Provided by Our Listed CDMOs:
Advanced Gene and Cell Modification: Utilization of state-of-the-art techniques for precise gene editing and cell modification to develop effective therapies. This is a key service of cell therapy CDMO and CGT CDMO providers.
Rigorous Safety and Efficacy Standards: Strict adherence to safety and efficacy standards, ensuring the highest level of patient safety and therapeutic effectiveness. This is crucial in cell therapy CMO services.
Scalable Manufacturing Solutions: Capability to scale from research-level batches to commercial-scale production, catering to the growing demand for gene and cell therapies.
Regulatory Expertise: In-depth understanding of the regulatory landscape governing gene and cell therapy products, ensuring compliance with FDA, EMA, and other regulatory bodies.
Comprehensive Development Services: From concept to commercialization, providing end-to-end development services including process development, clinical trial material production, and commercial manufacturing.
Your Partner in Revolutionary Treatments
Pharmaoffer connects you with CDMOs that specialize in gene and cell therapy production, essential for the new era of treatment paradigms. Our platform ensures you have access to partners with the expertise and infrastructure necessary to drive forward these groundbreaking therapies.