美国Progenitor Cell Therapy (PCT)
Progenitor Cell Therapy (PCT) 是一家以客户为中心的服务企业，为细胞疗法的开发与推广提供支持。PCT 提供符合 cGMP 标准的细胞生产与咨询服务，满足监管、金融、技术、工艺和质量体系战略。该公司提供与工艺和产品开发、验证、尽职调查、评估、组织采集、处理以及存储、产品生产、分销与运输相关的全方位支持与咨询服务。

 The Partner of Choice for the Development and Manufacturing of Cell Therapies

Progenitor Cell Therapy (PCT) is a client-based cell therapy services company that supports the development and commercialization of cellular therapies. PCT provides cGMP-compliant cell manufacturing and consulting services that address regulatory, financial, technical, process, and quality system strategies. Services include a full spectrum of support and consulting related to process and product development, validation, due diligence evaluations, tissue collection, processing, and storage, product manufacturing, distribution and transportation.

Click here for a PDF copy of the PCT brochure

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Click here for a PDF copy of PCT's corporate overview presentation

Our Commitment
We have a long term commitment to the development of effective cell therapies as the emerging paradigm for the treatment of disease. Our unique and wide-ranging experience spans the entire spectrum of cell therapy product development from research to processing and manufacturing, and from regulatory and quality compliance to clinical application.

Our team of professionals is prepared to offer their expertise to support your product development needs, from pre-clinical and clinical research and development, to regulation, accreditation, reimbursement and the commercialization for cellular therapies.

Our Service Product
To date, Progenitor Cell Therapy has processed more than 3,000 cellular products for over 1,000 patients and provided cost-effective cell therapy manufacturing services from our cGMP clean room facilities in Hackensack, New Jersey and Mountain View, California.

Our two facilities consist of clean rooms, cryopreserved cellular inventory, and a Quality Control/Testing laboratory capable of performing flow cytometry, thermal cycling (PCR), ELISA, microbiology and cellular morphology analysis.

Our facilities, processes, and personnel are in compliance with the cGMP and cGTP regulations, the standards of the FDA, FACT, AABB, and are accredited by the following organizations for various purposes:

The Foundation for the Accreditation of Cell Therapy (FACT)
The College of American Pathologists (CAP)
AABB
Progenitor Cell Therapy provides door-to-door cell transportation services within the continental United States for environment-sensitive and time-critical packages. We have partnered with a specialized package delivery airline and network of ground couriers.

For those looking to engage in clinical trials, Progenitor Cell Therapy also has access to a large patient population base and a wide range of clinical protocols in cell therapy. These clinical protocols include Investigator New Drug (IND) and Investigational Device Evaluation (IDE) developed with and by Progenitor Cell Therapy for the clinical evaluation of its client's products.

Progenitor Cell Therapy has developed mechanisms, processes, and expertise to confer the highest likelihood of success for development of cell-based products at any stage in the developmental pathway.