At 2Richards, we believe in the power of teamwork. With over 65 years of combined experience in clinical development, we are well-prepared to assist you in the following GCP areas:

• Preparation for and management of regulatory inspections

• Deployment and continuous improvement of risk-based quality management systems

• Advising on complex compliance questions

• Interim GCP-QA Management service

• Delivery of GCP and inspection-related training

We have assisted over 70 organizations, from small start-ups, through medium-sized organizations poised for commercialization, and multinational biopharmaceutical organizations with large portfolios in a diverse range of therapeutic areas.

We have experience in trials conducted globally with small molecules, biologics, gene therapies, and drug-device combinations. 

2Richards use our extensive industry experience to provide practical, risk-based approaches to managing compliance with GCP regulations, focusing on patient safety and data integrity to ultimately ensure that resources are applied to what matters most. 

Ready to see how we can help you? Reach out to 2Richards!