RevereIT LLC: Providing Cost Effective Business Solutions to Pharma and Life Sciences

The pharmaceutical industry is constantly encountering unprecedented business challenges in terms of rising costs, reduced reimbursement, growing consumerism, and increased government regulation. Keeping this constant and aggravating issues in focus, Andy Gupta is leading RevereIT, an end to end consulting and solutions company to help pharmaceutical firms deal with their business challenges. Recommending wise IT investments and fundamental changes to business models, RevereIT helps its clients to reduce cost, streamline administrative processes, improve quality of care and increase the speed of new discoveries to market.

Headquartered in Herndon, VA, RevereIT specializes in Regulatory Affairs, Technical Writing, QA/QC, Clinical Operations, Computer Systems/Equipment/Cleaning Validation, Clinical Research, Project Management, and Business Development. “Our Quality Assurance and Regulatory Compliance group provides customers with unparalleled industry experience,” says Gupta.

RevereIT’s project delivery team possesses the best in life science talent and capabilities, which aligns to each of the customer’s unique business, compliance and technology needs. “We have successfully executed hundreds of projects in life sciences, across all of our practices. Our project teams deliver to the customers’ planned milestones and project deadlines, helping them save time, and money,” says Gupta. RevereIT’s on-board team adds value by fulfilling client’s project-based business requirements with its technological skills, business acumen and cultural experience. Since its inception, RevereIT is providing consulting services to the Pharmaceutical, Life Sciences, Healthcare, Energy, Manufacturing, Medical, Biotech, and Telecommunications sector. For the pharma sector, the company provides its services with particular attention to pharmaceutical validation and software quality assurance. In the validation area, RevereIT’s experience span across qualification of single pieces of equipment to entire facility validations including utilities, equipment, processes, and computerized systems.