NVIDIA’s $250M, five-year compute donation funds UK agentic AI safety research, with implications for how GMP teams validate and govern autonomous AI.
News|Articles|March 2, 2016
TxCell Launches Industrialization Laboratories and Technology Transfer Academy
Author(s)Pharmaceutical Technology Editors
TxCell’s new facilities are based in Sophia Antipolis, France, on the premises of GenBiotech.
Advertisement
TxCell, a biotechnology company developing personalized cellular immunotherapies using regulatory T-cells to treat chronic inflammatory and autoimmune diseases, announced the launch of its new process industrialization laboratories and technology transfer academy facilities in Sophia Antipolis, France, according to a Feb. 29, 2016 press announcement. The new facilities will be based in Sophia Antipolis, on the premises of GenBiotech, an affiliate company of the Genevrier Laboratories.
According to the company, the facilities will be used to improve the existing TxCell manufacturing process for its ASTrIA platform, as well as development and manufacturing of its ENTrIA platform. The facilities will also host the TxCell Academy for Technology Transfer. The academy will be responsible for educating and training all contract manufacturing partners. It will also train future strategic partners on the manufacturing processes of TxCell’s personalized cellular therapies.
Source:
Advertisement
Related to this article
Richard Jaenisch explains what FDA's real-world use case database means for CMC and quality teams navigating NAMs.
This article examines how modern automation platforms create the digital foundation required for Pharma 4.0 by integrating manufacturing systems, centralized data management, Industrial Internet of Things connectivity, electronic batch production records, and AI-driven analytics.
Ron Scarboro, Azurity Pharmaceuticals, explains how cross-functional development, disciplined reformulation, and post-approval metrics can help proven medicines work in everyday use.
This week, drug formulation and manufacturing experts showcased their knowledge, and companies exhibited their products, at CPHI Milan.
FDA approves Teva’s Weltruza, a once-monthly subcutaneous olanzapine for schizophrenia whose copolymer depot eliminates post-injection monitoring.
Mitigating nitrosamine risk requires assessing each product individually, says Bram Baert, Global Head of Regulatory Affairs at Capsugel, and Sandrine Picco, Senior Analytical Specialist on Capsugel's Innovaform Accelerator Team, in this interview with PharmTech.
Jason Bertola, executive director of Commercial Development for the Advanced Synthesis Platform at Lonza in North America, explains the demand for spray drying and the hurdles involved with scale up, in an interview with PharmTech.
Advertisement
Advertisement
Trending on Pharmaceutical Technology
1
Q&A: Patient-Centric Drug Development Should Start at Product Definition
2
Clinical Trial Delays: FDA’s Expedited IND Pilot vs China’s 818 Decree
3
PharmTech AI Pulse Check: AI Watermark Vulnerability
4
Pritelivir Shifts Resistant Herpes Care from Intravenous to Oral
5