In the previous blog, I discussed the importance of using purpose-built software. Because we are a purpose-built EAM solution provider, we s...
Now that we’ve covered broader GMP issues in the previous 3 blogs, I want to discuss the overall role of an EAM/CMMS in managing compliance ...
In the previous blog in this series, I discussed the FDA’s new Office of Pharmaceutical Quality and its overarching goals. There is no bette...
The Office of Pharmaceutical Quality (OPQ), launched in 2015, will be used to carry out the FDA’s long term plan to establish a uniform qual...
In our previous blog series, we briefly explored the growing enforcement of the FDA. From 2007 to 2012, the number of warning letters given ...
So now that we have discussed the top considerations when implementing a multisite software solution, we are going to cover the benefits and...
Going mobile is the key differentiator in driving paperless asset management (whether EAM, CMMS or CCMS). This is mostly because the use of ...
Mobile Form Factor in a Paperless Environment Now that we have covered the benefits of leveraging technology for maintenance and calibration...
In our previous blog, we discussed the benefits of leveraging technology for maintenance and calibration along with some of the necessary co...
Several factors have recently come together to make going paperless a realistic investment for many companies. In this series of blog posts,...
