Patient safety is paramount when performing clinical studies or using pharmaceutical products or medical devices. By applying Good Practices (GxP), quality guidelines and regulations, companies within the healthcare and life sciences industries can ensure their products are safe for use.
Whether you are a start-up company in need of professional expertise to set up and implement a business model for Quality, Validation, and Compliance, or a global life sciences company in need of resources to execute and manage validation and compliance projects, CTG’s Regulatory Compliance (RC) practice is fully equipped to get the job done and satisfy your expectations. Our services are based on lean, scalable, risk-based, and agile concepts, and were designed using industry best practices.
Compliance Assessment and Remediation
Agile Computer System Validation
To learn more about CTG's GxP services, view our service offering collateral.
Our services are based on lean, scalable, risk-based, and agile concepts, and were designed using industry best practices.
Our Validation Consultants play a pivotal role in assessing, implementing, remediating, and maintaining GxP Compliance in your organization. We invest heavily in the rigorous training, skill, and competence development of every consultant, which results in expertise across many different business domains, including:
Proficient in the fields of science, combined with deep information technology, information security, and validation expertise
Achievement of critical certifications, such as Project Management, CISM, ISO 27001 Lead Implementer, ISO 22301 Lead Implementer, and more
Our strong, strategic partnerships have allowed us to better serve the needs of our clients for more than 50 years.
Given the accelerated pace at which new technologies emerge and the specialized and evolving needs of our clients, it’s essential that we leverage industry partnerships to amplify the value we provide to clients.