Regulatory Affairs & Quality Management Services

We have a successful track record of regulatory submissions for Medical Devices, In Vitro Diagnostics, Software as a Medical Device (SaMD), Drug-Delivery Systems, and Device-Led Combination Products. We work with FDA and major Notified Bodies and Competent Authorities/International Regulatory Agencies worldwide to determine the optimal regulatory pathway for your product, minimizing potential obstacles. Our approach is pragmatic and efficient, enabling you to achieve your commercial objectives quickly, while confidently meeting all necessary regulatory requirements.

Regulatory bodies require traceable processes and documentation to ensure quality, performance, safety, and effectiveness of medical devices. We have a long history of expertise designing Quality Management Systems that align with the risk and complexity of your device, your organization's needs, and specific performance and customer requirements.

We focus on achieving consistent quality compliance while ensuring that your products meet regulatory standards and work closely with you to create a tailored Quality Management System that is efficient, effective, and scalable to support your business goals.

Manufacturers must objectively demonstrate the safety and performance of a medical device before bringing it to market. This evidence, unless duly justified, must originate from thoroughly designed and executed (pre- and post-market) clinical activities to provide evidence that the device performs as claimed. Our Clinical Research Organization (CRO) services bring decades of experience in medical device engineering, quality, and regulatory affairs, to support all aspects of your project comprehensively.

Medical device and IVD regulations often require local presence to place products on the market. With multiple global offices, Veranex helps you navigate the regulatory requirements for each, acting as your designated local representative or agent and assisting you in meeting all regulatory requirements.

A comprehensive risk management strategy not only supports patient and user safety but also appropriate verification and validation activities, and implementation of effective and efficient processes. We partner with your teams to implement a risk approach throughout the life cycle of your Medical Device or In Vitro Diagnostics (IVD) Device.

Having worked within the FDA, Notified Bodies, larger organizations, and nimble start-ups, our subject matter experts bring a wide array of specialization to each project they work on. This ensures the delivery of timely, superior project results in areas such as Software, Cybersecurity, Electrical Safety, Biocompatibility, Sterilization, and more.