Since its founding in 1994, QPharma® has been at the forefront of regulatory compliance consulting for the life sciences industries. Headquartered in historic Morristown, New Jersey, and neighboring many of the world’s top pharmaceutical, medical device, and life sciences firms, QPharma commands respect throughout the industry for its commitment to superior service.
QPharma’s Professional Services division is renowned for its skill at helping clients efficiently and cost-effectively navigate the challenges of remediating quality and compliance issues. For example: in response to FDA action, QPharma was engaged by an external overseer and the CEO of a leading pharmaceutical company to oversee a major remediation program across two states and seven validation categories. As a result, the warning letter was satisfied, and FDA elected not to pursue further action. This is just one of hundreds of success stories experienced by our clients.
Every solution is built on a firm foundation of quality and regulatory compliance, enabling clients to pursue commercial success while adhering to complex regulations enforced by FDA, CMS, and other agencies. Whether working with a brand team to launch a new product or developing and implementing major remediation activities for a manufacturer under FDA consent decree, QPharma fulfills its role as a trusted partner to its valued clients.