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August 16, 2023 | ValGenesis and AUSTAR implemented ValGenesis iRisk at two large drug manufacturing centers in China, strengthening compliance across their operations.
Global Biotechnology Company Selects SaaS-based ValGenesis VLMS To Digitalize Validation Lifecycle Processes
ValGenesis and Radiant Digital PTE Ltd. are poised to deliver future-ready solutions that can completely transform a company's IT systems and applications, infrastructure, and workforce.
ValGenesis’ platform, which includes its flagship VLMS offering, helps the world’s leading life sciences companies enable compliance and enforce standardization with 100% digital, risk-based validation software.
ValGenesis and Life Science Consulting Pvt. Ltd. will expand technical and regulatory support to customers through a network of experts across the globe, delivering new levels of digital collaboration, data integrity, risk management, and quality and compliance across validation lifecycle processes.
Leading pharmaceutical company in Brazil selected ValGenesis iRisk to redefine and automate the company’s risk-based validation processes.
KVS Technologies is highly proficient in computer system validation (CSV), and regulatory intelligence and compliance services, helping companies stay current and compliant with 21 CFR Part 11 and EU Annex 11 regulations.
An elite biotechnology company selected ValGenesis VLMS for digitizing multiple validation processes across the organization. The company selected ValGenesis VLMS after a rigorous audit of solutions.
ValGenesis, Inc., the market leader in enterprise Validation Lifecycle Management Systems (VLMS), and MEPHARMA, a strategic regulatory consulting services company, have partnered to provide a range of regulatory intelligence, compliance, and validation and automation solutions for companies in the United Arab Emirates (UAE) and the Middle East and North Africa (MENA).
ValGenesis Process Manager is designed to eliminate these commonly cited observations by digitizing, automating, and controlling the end-to-end cleaning validation lifecycle, all aligned to the FDA's lifecycle approach for cleaning validation.