Displaying 1–19 of 19 results for DPT
When it comes to drug development and commercialization, Contract Pharma is bringing the brains and the brawn to do Pharma’s heavy lifting
DPT Laboratories and Confab announced their integration under the leadership of Paul Johnson
Managing the Complexities of Global Pharmaceutical Sourcing
What is Quality by Design (QbD) and Why Should You Care?
Aseptic Manufacturing: A Roadmap to Excellence
DPT Laboratories received notification from the U.S. Food and Drug Administration on February 19, 2013 that signaled the completion of their evaluation of DPT's corrective actions taken at its Lakewood, NJ facility
With the FDA's heightened focus on safety, regulatory agencies are increasing their presence in the manufacturing arena to ensure Current Good Manufacturing Practices cGMP are top of mind, and sponsors are placing greater responsibility for meeting cGMP requirements onto their outsourcing partners.
This white paper aims to provide a comprehensive overview of the CMC guidance by the U.S. Food and Drug Administration and present a streamlined approach for development and manufacture of nasal spray products. It will focus on the ability of the spray device to deliver reproducible plumes and ...
Lean Six Sigma, expertise in microbiology, and shop-floor experience all contribute to running a flexible, efficient contract facility, says DPTs new director of sterile ops.
DPT Laboratories Ltd. spent more than $30 million to upgrade its sterile pharmaceutical manufacturing capabilities in Lakewood, N.J. The company invested in a new water system for injection, clean steam and HVAC systems and a new microbiology laboratory. The lab allows for in-house microbiology ...
Corrective and Preventive Action (CAPA) management is vital to an organization's regulatory compliance initiatives. DPT Labs shares best practices from a recent implementation.
Despite a tough economy, few question the value of attending Interphex, and this years show promises to be as good as ever.
Clearly worded contracts are essential, wherever your contract partner is based. Dr. Eize de Boer of SGS spells out the requirements.
Drugmakers are using MES and ERP more effectively and harnessing the power of new data acquisition tools.
Prized for benefits that include reduced toxicity, controlled release and the manufacturability issues it raises is being considered much earlier in drug development process.
Despite the buzz about "process understanding" and PAT, vaccine manufacturing remains defiantly un-PAT-able and an extremely risky business. Chiron's recent Fluvirin case offers important lessons in due diligence, quality management, and GMPs. However, it also points out an urgent need for ...
DPT Laboratories is recognized globally for its technical expertise in semi-solid and liquid research, development and manufacturing services for the worlds leading pharmaceutical, biotechnology, and healthcare companies. This wealth of expertise has helped to establish DPT as one of the few ...