SeerPharma is pleased to announce a strategic partnership with QACV Consulting, enhancing our ability to support clients in the United States.
For over 35 years, SeerPharma has been at the forefront of supporting Pharmaceutical and Medical Device companies in the Asia-Pacific region on matters related to Quality and GxP compliance.
As our clients expand their operations and seek to navigate the complex regulatory landscape of the US FDA and other regulatory agencies, there is a growing need for quality oversight of manufacturing and supply chain activities in North America, as well as vendor oversight and governance for clinical and nonclinical studies and Pharmacovigilance activities.
Through this collaboration, SeerPharma clients now have direct access to a team of experienced Quality and GxP professionals based in the U.S. and Europe, ensuring seamless support in meeting FDA global regulatory requirements and expectations.
Likewise, SeerPharma will also support QACV clients requesting assistance in the Asia-Pacific region.
This partnership underscores our commitment to delivering comprehensive, globally integrated quality and compliance solutions. By working closely with QACV Consulting, we are expanding our network of industry specialists to better serve our clients in North America, Europe, and the Asia-Pacific region.
To learn more about QACV Consulting, visit: QACV Consulting
Initiatives such as this, are just another way we further our mission to “Advance Quality and GMP best practices” for our industry.