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Kneat Announces Selection by Top Ten Biopharma as the Corporate Solution for Global Manufacturing and Provides an Update on its Recent Financing

Kneat Announces Selection by Top Ten Biopharma as the Corporate Solution for Global Manufacturing and Provides an Update on its Recent Financing News provided by Share this article LIMERICK, Ireland, May 7, 2021 /CNW/ -  kneat.com, inc. (TSX-V: KSI) ( Kneat ) announces it has signed a five-year corporate Master Services Agreement (MSA) with another top ten biopharma company, and provides an update on its recent financing.   Top Ten Biopharma Selects Kneat as its Corporate Validation Platform for Global Manufacturing In December 2020, Kneat announced its SaaS platform was chosen by this research and development-focused biopharma leader for a single site. Today, we are pleased to announce it has selected Kneat as its corporate-wide manufacturing e-Validation platform. The company has more than seventy thousand employees across multiple operations in six continents,  and the selection of Kneat follows an extensive formal evaluation by the company s digital manufacturing soluti

ComplianceOnline Hosts Vendor and Supplier Qualification Program Seminar for FDA Regulated Industries

Vendor and Supplier Qualification Program for FDA Regulated Industries Vendor and Supplier Qualification Program for FDA Regulated Industries Seminar has been added to ComplianceOnline.com s offering. SAN JOSE, CALIFORNIA, UNITED STATES, April 19, 2021 /EINPresswire.com/ ComplianceOnline, the world’s leading provider of training for regulated companies will hold a virtual seminar entitled ‘Vendor and Supplier Qualification Program for FDA Regulated Industries.’ The seminar which will be presented by Joy McElroy, will help attendees establish and manage a program that is FDA compliant and robust. The FDA regulates manufacturers of medical products such as devices, pharmaceuticals, tissue products, and biologics. However, the regulations don’t usually extent to suppliers. Instead, the FDA expects the medical product manufacturer to implement an effective program to qualify and re-qualify suppliers for these regulated industries.

IPC Launches IPC-CFX Self-Validation and Equipment Qualification Systems

IPC Launches IPC-CFX Self-Validation and Equipment Qualification Systems IPC has introduced IPC-CFX Self-Validation and Equipment Qualification Systems. The IPC-CFX Self-Validation System is a cloud-based test bed for equipment vendors and manufacturing facilities to self-validate CFX messaging. The Equipment Qualification System establishes a CFX Equipment Portal with independent third-party validation of equipment. The IPC-CFX Self-Validation System ensures CFX connections, broadcasting, and consumption of CFX messaging. The self-validating system will confirm the correct network identification and subscription messages and that all relevant topics (mandatory and optional messages) are supported. It will ensure message content data integrity and that messages are sent and responded to. The cloud-based system is offered as an annual subscription but can be purchased in quarters as well. The service allows access t

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