Articles and News
371 Results Found
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Siemens to automate GlaxoSmithKline
Siemens will become a strategic partner of GSK in manufacturing automation and thus the preferred automation supplier for GSK production and R&D sites worldwide. -
Endress+Hauser signs Eastern Controls as rep
Eastern Controls is now the E+H rep for the Mid-Atlantic area – Metropolitan New York, Eastern Pennsylvania, New Jersey, Delaware, Maryland, and Northern Virginia. -
Werum to supply MES to Losan Pharma
PAS-X MES will be implemented in several stages and it will be interfaced with the Infor Blending ERP system. -
Four Factors Driving the Global Industrial Dispensing System and Equipment Market
Global industrial dispensing system and equipment market was valued at USD 12.85 billion in 2014, growing at a CAGR of 7.0% from 2015 to 2021 to account for USD 20.57 billion in 2021. -
OPC forms working group to fight counterfeiting
The Steering Committee of the Open Serialization Communication Standard Working Group (Open-SCS) addresses compliance to healthcare counterfeiting regulations. -
Collaborative Robots Transform Industry
Bill Lydon: I am convinced that collaborative robots are the highest impact automation development to improve manufacturing since the assembly line. If this development follows the cost performance trends of past developments, like PCs, we at the beginning of a new revolution. -
Robot use increases more than 27% in 2014
By Bill Lydon, Editor According to IFR, more than 220,000 robots were sold globally in 2014. The automotive industry is still the strongest, followed by the electronics industry. But there are many more applications in other industries that are just starting to grow, particularly with new small, safe, and collaborative robots. -
Endress+Hauser files 259 patents in 2014
Endress+Hauser employs more than 700 people in research and development. -
Endress+Hauser hits 2 billion euros in sales
In 2014, Endress+Hauser increased net sales by approximately 11 percent, exceeding the 2 billion euro mark. -
ACM Facility Safety and Endress+Hauser Announce P&ID Interpretation Workshop
This 2-day course gives students the ability to read and understand P&IDs for the analysis of emergency situations; and for safety, environmental and regulatory compliance issues such as Process Hazards Analysis and HAZOP studies. -
Omnity PLM software helps Cytonome purify cells
Cytonome produces cell purification systems and needed to achieve bi-directional seamless communications among engineering, manufacturing and purchasing. PLM software helped. -
HMI simplifies FDA and USDA compliance reporting
By: Julio Delgado, Stock America HMI software from InduSoft provides eSignatures, database connectivity and other features vital to proper process validation and compliance with food and pharmaceutical regulations. -
Registration opens for ISA Food & Pharmaceutical Symposium
ISA opened attendee and exhibitor registration for its 2015 Food & Pharmaceutical Division (FPID) Symposium, which will be held 9-11 February 2015 in Philadelphia, Pennsylvania, USA. -
Octapharma adds Track & Trace software at pharma plant
Octapharma, a manufacturer of human protein products, is using the PAS-X Track & Trace Serialization Aggregation solution in Vienna. -
Addressing FDA CFR Regulation Compliance with Cloud based ERP Software
By Bill Nolan, Rootstock Software Many regulated manufacturers use paper-or Excel-based processes to address compliance. For discrete manufacturers who are required to have FDA CFR compliance, the Salesforce1 Platform connected an ERP system offers some distinct advantages. -
Belden says Dragonfly Malware Targets Pharmaceuticals
Research that shows the recently revealed Dragonfly (Havex) malware is likely targeting the pharmaceutical sector, not the energy sector as previously believed. -
MAVERICK Acquires CQS Innovation
CQS Innovation is a Michigan-based systems integrator specializing in control and information systems for life sciences, chemical and metals industries. -
Taming the pharmaceutical validation dragon
By Robert Harrison, COPA-DATA It takes an average of twelve years and over £200m to get a new drug from the laboratory onto the shelf. As a result, the pharmaceutical industry is well known for its prudence, especially regarding the uptake of new technologies. Here’s how appropriate technologies can help, rather than hinder, essential regulatory compliance including ISO 50001 and FDA 21 CFR Part 11. -
UNIGEN starts up Werum's PAS-X MES in only four months
PAS-X was delivered with the entire user interface in Japanese. Werum carried out this project in cooperation with their Japanese integration partner CST Chiyoda System Technologies.

