It is imperative that Pharmaceutical companies have a good handle on how to perform Product Quality Reviews (PQR). In fact, effective PQR’s are necessary in demonstrating GMP compliance to regulators such as the TGA and FDA (Annual Product Review).
We invite you to attend our inaugural SeerPharma Symposium, which will be held at the Park Hyatt, in Melbourne on Friday the 20th of May.
After 25 years of serving pharmaceutical and medical device professionals in the Asia-Pacific region, we would like to bring all of you under the one roof. With this in mind, we’d like the day to focus on “How...
How do you Tackle Human Error within a GMP Environment?
March
03,
2016
Your quality systems and procedures are in place, however no matter how much you try, people still don’t fully comply with them. These deviations and subsequent investigations lead to lost productivity. Typically, manufacturers identify “human error” as the root cause and assign corrective actions to train/re-train the team.
