INFOGRAPHIC: A snapshot of how SeerPharma has supported its clients in 2016 on matters of QA and GMP compliance.
A major pharmaceutical distribution organisation engaged the services of SeerPharma (Singapore) Pte Ltd to provide a review on the compliance of its core SAP-Centric solution to the GxP Computer Systems Validation (CSV) requirements of both FDA 21 CFR Part 11 and PIC/S Guide to GMP Annex 11. There were 2 phases to this project.
One of our senior consultants in Singapore, received the following glowing recommendation from the Sri Lanka Pharmaceutical Manufacturers' Association (SLPMA) which is a testament to the quality of our team in Singapore who continually strive to deliver exceptional service to customers in the region.
