RevereIT LLC offers a wide range of IT services to its clients to conquer the technological edge. We provide our clients with the best available strategic advice and knowledge support.

Our solution providers specialize in a wide range of technologies, processes, products & operating systems and have experience in proven methodologies to optimize legacy systems and to integrate them with leading-edge technologies.

RevereIT LLC offers smart solutions for its clients for all their technical requirements. We provide solutions to our clients at a very competitive rate. Our team is wise, creative and enthusiastic, and challenges the latest technology. RevereIT LLC is committed to providing the best resources and solutions to our clients. We maintain win-win relationships with our clients. We firmly believe that our success depends on your success.

Regulatory Compliance- Are you ready for the stringent standards and Strict timelines? RevereIT LLC can help you meet your deadline! The pharmaceutical industry is faced with unprecedented business challenges: rising costs, reduced government reimbursement, growing consumerism, and increased government regulation, such as 21 CFR Part 11, QA/QC, Computer System Validation, HIPPA.

Our Quality Assurance and Regulatory Compliance group provides customers with unparalleled industry experience. By making wise IT investments and fundamental changes to business models, Organizations can reduce their costs, streamline administrative processes, empower consumers, improve quality of care and increase the speed of new discoveries to market.

Partnering with many of the major Pharmaceutical, Biotech companies and Specialist consultancies to help them to exceed their regulatory obligations, RevereIT LLC is rapidly becoming the market leader in providing smart solutions in the Validation & Regulatory Compliance market.

 
Computer Systems Validation

Computer System Validation (CSV) in regulated operations provides confirmation by examination and provision of objective evidence.

Validation for Vaccine Manufacturers An Introduction

This guidance document has been prepared to aid vaccine manufacturers in the preparation and performance of the validation studies required by GMP.