Verista is a nationwide industry leader in providing quality and compliance related consulting services to regulated Life Science industries including pharmaceutical, biotech, gene therapy, petroleum and food companies. These services focus on computer systems validation, commissioning, qualification, validation of manufacturing automation and packaging solutions, serialization, machine vision, FDA verification, data integrity and change management support. The Company is headquartered in Fishers, Indiana with additional local offices in Pennsylvania, Massachusetts and California.
Regions Covered: Alabama, Alaska, Arizona, Arkansas, California, Canada, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming
Services Offered: Asset Creation (create the asset in RAM), Asset Description (drive consistency for asset descriptions), Asset Hierarchy (parent, child relationships in RAM), Asset Nomenclature (drive consistency for asset naming nomenclature), Asset Walkdown (identify asset Mfg., Model, Serial), BMRAM CMMS Support (On Site Staff Augmentation), BMRAM CMMS Support (Virtual), BMRAM Config Workbook, BMRAM Data Migration Workbook, Cal. / PM Load Leveling (load level schedules based on business needs), Cal. Initial Assesment, Cal. Interval (risk based), Cal. Interval Assessment, Equipment Quailification, MDT Creation, PM Initial Assessment, PM Interval (risk based), PM Interval Assessment, PM Task Creation, Software Validation, SOP’s (BMRAM user, admin, Mnt. Prgm, Cal Prgm, etc.), URS, FS, IQOQPQ, Change Control
