Compliance Services

PharmaSys can provide your company with general compliance services. We have many years of experience in pharmaceutical manufacturing and quality assurance. We can help you comply with cGMPs, GLPs, and GCPs by developing standard operating procedures, developing QC sampling programs, developing validation programs and performing audits.

Capabilities

At PharmaSys, compliance is #1. We have built our reputation on providing cost effective compliant solutions to our customers when regulatory changes necessitate. Our professional staff has many years of experience in the FDA regulated industry. We can help you comply with cGMPs, QSR, GLPs, and GCPs by developing:

• Master Validation Plans
• Policies and Procedures
• Quality Systems
• Validation Programs
• Remediation Plans
• Training Programs
• 483 Responses
• Warning Letter Responses

In addition to the development of compliance solutions, PharmaSys can act as an independent auditing agency to provide you with that extra level of comfort that your systems are meeting the current industry standards and regulations. Whether it’s a one time audit or a recurring periodic audit you can be assured PharmaSys will listen to your needs and keep the focus where it belongs - on your requirements.

You have the problems identified, compliant solutions have been developed - now what? PharmaSys will assist you with the implementation of the solutions. Our involvement can be minor or major, based on your specific needs.

If you are interested in finding out more about PharmaSys' world-class offerings, complete and submit the form provided below. You will be contacted to discuss your needs and provided with information about how PharmaSys can help you achieve your compliance and validation goals.