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In our previous blog as part of this CQ Guide Series of migrating your QMS to the cloud, we share 8 reasons WHY you should move your QMS to the cloud. The blog also detailed the journey of how a fast-growing medical device manufacturer benefitted from the move away from legacy QMS software.
In this post, we focus on the following:
The next question is: How to make sure the migration process is done right? Quality leaders usually start with a small number of processes to migrate to the cloud. The migration could happen either from a set of legacy systems or a combination of manual processes. A well-defined product requirements document along with a detailed roadmap will really help.
We believe that the following five factors are critical to making sure the migration process goes as per plan:
So, when is the right time to make the shift? According to an article published by Gartner, legacy software is responsible for holding back business growth in several companies. As per a survey conducted by Hitachi Consulting, 9 out of 10 business leaders believe that legacy systems cause inefficiencies and drive up costs.
Cloud-based solutions are better suited for collaboration, mobility, and scalability. Also, cloud-first is the way to go to embrace next-generation technology like AI, ML, NLP, and advanced analytics.
Often, the trigger to migrate often comes from specific business requirements, like the following:
There could be several other reasons why you’re looking to move your QMS from on-prem to the cloud. But, all things considered, it is a no-brainer to make the shift NOW.
In fact, this should have been done yesterday!
Download it here: https://www.compliancequest.com/whitepaper/from-prem-to-cloud-qms/
“ComplianceQuest is amazingly robust and easy to use. We first started using CQ for Document Control but today we use it for Training, CAPA, Complaints, Change Control, Supplier Management, and Audit Management.
Our experience has been very positive from selection to implementation. The CQ solution is extremely powerful and has a variety of applications and modules. Configurable reporting and dashboarding features allow for ease of communication and transparency of data within the company. All processes are electronically linked, adding both ease and traceability to interrelated QMS processes (I can launch a CAPA from my Complaint form!) (I can launch an Engineering Change Order from my CAPA form!). Configuration can be as simple or as complex, as you make it.”
Manager, Quality Assurance, Global Life Sciences Company
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