CVO CYBERCONSEIL VALIDATION ORGANIZATION

Owners

Goods & Services

Education services for chemical and pharmaceutical industry in the nature of classes and seminars pertaining to computerized systems validation, equipment and process validation ; to quality systems management and regulation compliance ; to engineering related activities, namely, project management, specification management, commissioning management

Consulting services for chemical and pharmaceutical industry regarding computerized and non-computerized machine, apparatus, and instrument testing, computer systems equipment testing and computer systems operating process analysis and evaluation, quality assurance services in the field of computer systems operation and equipment, regulation compliance, engineering related activities, namely, computer project management and construction project management in the nature of architectural design supervision, and regarding computer systems user requirement specifications, computer operations functional specification management, software and equipment tests; reviewing standards and practices to assure compliance with United States and European chemical, pharmaceutical, food, drug, manufacturing, medical, electrical engineering regulations, standards and guidelines; software design and development for chemical and pharmaceutical industry for the purposes of facilitating computerized systems testing, computer systems equipment testing, and computer systems operating process analysis and evaluation, quality assurance services in the field of computer systems operation and equipment, regulation compliance, engineering related activities, computer project management and construction project management, computer systems specification management, factory acceptance testing management and site acceptance testing management

Database program for facilitating, in the chemical and pharmaceutical industry, the entire validation process from the selection of the initial applicable regulatory texts, through the generation of protocols, to qualification and validation reports ; and for facilitating the consultation of all regulatory requirements and the selection of the articles applicable to a project.