For more than 35 years, SeerPharma has been a trusted partner to pharmaceutical and medical device organisations across the Asia-Pacific (APAC) region, providing expert guidance on Quality Management Systems (QMS) and Good Manufacturing Practice (GMP) compliance.
At the heart of our work lies a team of highly experienced quality and regulatory...
With the ever-evolving advancements of computerised systems and their involvements in the pharmaceutical, medical device, biotechnology and clinical trial industries, it is more critical than ever to ensure that these systems are appropriately assessed, validated and controlled. This is essential to safeguard the ensuing data integrity, product...
SeerPharma has a long-standing reputation for helping pharmaceutical and medical device companies establish new or upgrade existing GMP manufacturing facilities. The team is currently engaged in multiple facility projects across the APAC region, working on complex facility projects involving the manufacture of:
Copyright © SeerPharma
