Learn how you can save up to 25% in potential savings with our integrated approach to product maintenance
Achieve Better Patient Outcomes with an Integrated Approach
In the midst of ever-evolving regulatory standards and increasing cost pressures, patient safety must always remain the top priority. Ultimately, product and patient safety are tied to product value, but a commitment to safety shouldn't mean sacrificing cost-efficiency. Quintiles can help you transform pharmacovigilance into a competitive advantage.
We help you manage global regulations and post-approval safety deliverables while gaining a deeper understanding of your benefit-risk profile. Our optimized processes, technology and resources ensure quality and save you money – now and moving forward. Lifecycle Safety is centered on your needs and adapts to grow with you.
Our dependability is shown in the numbers
- Quintiles Global Safety and Pharmacovigilance has processed almost 1.5M clinical, post-marketing and medical device safety reports globally over the past 5 years with over 99% on time compliance to sponsors and regulatory agencies.
- Quintiles has delivered more than 450 aggregate safety reports between January 2013 and August 2014.
- Quintiles has delivered >220 standalone benefit risk assessment reports between January and September 2014.