There’s a lot of pressure coming at you from every direction to comply with FDA regulations. You’re required to have the right technologies and policies in place, but this can be overwhelming and time-consuming for a business owner with an already overflowing plate. In order to operate within FDA compliance, you need a partner that provides expert IT solutions. Luckily, our founders have extensive experience providing FDA compliance validation for businesses just like yours.
We provide a complete range of compliance solutions for companies regulated by the FDA. These solutions include risk assessments, gap analysis, validation planning and remediation. Our technicians know that a solid Validation Master Plan (VMP) is one of the key documents for ensuring that a computer system or architecture meets the requirements for compliance. We ensure that your VMP provides an auditor with your company’s validation strategy and guiding principles. So, whether it’s the implementation of a new system or an audit and remediation of an existing application, Information Age Systems has you covered. We utilize the principle outlines for Good Automated Manufacturing Practices (GAMP) to help you adhere to computer systems validation requirements.