VQS – Validation Expert

VQS has a vast amount of experience in the pharmaceutical industry. In most cases our experts can execute your statement of work in a fraction of the time it would take a team of people to accomplish. We can do this without disrupting your environment. We bring the skills to produce all project deliverables..

  • Validation – CSV, Laboratory, Devices, Process, Product, Cleaning, IT, labs
  • Commissioning/Qualification – Facilities, Utilities and Equipment
  • Quality Risk Management – Identification, Analysis, Evaluation, Reduction
  • Quality/Compliance – Policies, Manual, Standards, Procedures, etc.
  • Quality Systems – CAPA, Audits, Metrics, Risk, Change Control, Incident Mgt
  • Regulatory Affairs – CFR, Standards, ICH, MHRA, USPs, Guidance’s

VQS provides staffing for both short and long term projects. We can serve as an extension of your staff to help support and manage your project objectives. We know the regulations, standards and Best Practices for launching and maintaining your products integrity. We take a risk based approach and validate against requirements that gets your products approved.

Our Books

Governing Cloud Computing
( Book 1 )

The federal government is not in the business of developing new technologies, but they are in the business of investing in them. If you are planning to develop, computer-based products and Read More

Price $64

Computers, Information and Laws
( Volume 2 )

Regulatory Agencies have developed a set of expectations for companies who develop and operate computer systems in regulated spaces. Read More

Price $122

QUALITY STATEMENT




" If you are not completely satisfied with our work
your next validation project is on us "