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.