MQA Updates
The start of 2015 sees a transition from working with Custom Pharmaceuticals to working with Dr.Reddy UK on the importation/packing of solid dose product. MQA Solutions have also had the opportunity to work with Pharmig and NSF DBA. 2015 is a year where there are...
MQA Updates
As we approach Christmas and the end of 2014 there is time to reflect on the changes in our industry. The year has seen the introduction of new guidance for QC Laboratories and Chapter 6 and the increasing importance of Data Integrity throughout all aspects of...
MQA Updates
I am delighted to report that I have had the opportunity to work with Brighton University as an honourary lecturer on their MPharm and MSc courses. The course content has been delivered as a range of lectures and workshops on QA and the role of the QP in the...
MQA Updates
The FMD is now a legal requirement and a full update was provided at the MHRA conference in December. The focus on API audits and GDP were discussed as was the requirement for excipient GMP. Both these activities are placing demands on pharmaceutical manufacturers and...
MQA Updates
The 2/7/2013 deadline has passed for the Falsified Medicines Directive and the need requirements for API manufacturers outside the EEA. Check out the MHRA web site for those countries ‘white listed’ and those requiring Letters of Confirmation. Focus is now moving...
