by Savannah Evans | Apr 9, 2018 | Getting the Most from Blue Mountain RAM
It is a requirement for organizations to track changes in a GMP environment. Effective and efficient change control processes are key to achieving quality and compliance. At this month’s Blue Mountain Customer Lab, we took a few polls of our audience to determine how...
by Savannah Evans | Feb 13, 2018 | Getting the Most from Blue Mountain RAM
At February’s Blue Mountain Customer Lab, we discussed how workflow management is a major driver for compliance and productivity. Therefore, a powerful workflow automation engine is a key component of an effective and compliant paperless system. Blue Mountain...
by Savannah Evans | Nov 11, 2016 | Industry Insights
Pharmaceutical compounding as we know today has grown exponentially since its origin – creating greater complexities than ever before. Drug compounding was once the job of local community pharmacists – preparing personalized medications based on patient-specific...
by Ginny Lee | Jul 11, 2016 | Industry Insights
More recently, the FDA has begun seeing data integrity as a major concern to the violations discovered during audits. As a result, the FDA published its new draft guidance, Data Integrity and Compliance with cGMP, in April 2016 with the purpose to provide...
by Savannah Evans | Jul 7, 2016 | Industry Insights
Implications of the Historic Brexit Verdict Since the final votes of the Brexit were counted, a majority of the UK’s decision to leave the EU has appeared pessimistic for the Biotech and Pharmaceuticals industries. As a result, there has been very little talk about...
