The SeerPharma team has been busy implementing electronic Quality Management Systems (eQMS) for a variety of companies ranging from pharmaceutical, nutraceutical, veterinary and medical device companies.
Clients have engaged with us to automate business processes and workflows to better manage their Training, Root Cause Analysis and CAPA processes. Using the modular nature of the software toolsets available, clients can scale-up to an entire eQMS solution over time; moving from a paper-based system to a paperless solution.
Start-up medical device companies have shown a genuine interest in a cloud-based solution that can assist with managing document control and design revisions of their medical device, to make their regulatory submissions simpler and easier.
Across the spectrum of Pharmaceutical QMS and Medical Device QMS requests, our team have been busy:
- Assisting with User Requirements Specification (URS) documents
- Designing and Configuring solutions to the clients' needs and
- Validating the platform once installed to ensure that it complies to the requirements set by regulatory bodies such as the TGA and FDA.
Contact us if you’re interested in moving from a paper-based quality management system / document control system to an eQMS paperless solution. We have a range of options and a plethora of experience with removing common headaches associated with a paper-based QMS.
This post comes from our April 2016 Journal. You may also be interested in this post:
