We provide efficient and cost-effective services of the highest quality. Our experience includes qualification of single pieces of equipment to entire facility validations including utilities, equipment, processes, and computerized systems. Our areas of specialization include the following:
  • Validation Master Plans
  • Protocol Development
  • Temperature Mapping
  • Utilities Qualification
  • Computer Software Validation
  • Electronic Records Compliance
  • Lab Facility Validation
  • Clean Room Validation
  • Cleaning Validation
  • Process Development
  • Process Validation
  • Gap Analysis
  • IT Network Validation
  • Test Method Validation
  • Training Programs

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. We have qualified Chemical Engineers, Biomedical Engineers, Bio-Engineers and Pharmaceutical Engineers.

 
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.