Panotica Hydra can be a modular QMS software for managing high-quality processes In line with the requirements of ISO 9001, 14001, 18001 together with other related ones. The software will allow not simply to collect all of the corporate’s advancement processes in one process, but also to actively combine all of the workers to the system platform.
We'll only keep personalized information for as long as essential for the fulfilment of Individuals needs.
Hydra gives usage of supervise functions remotely targeted at enhancing quality as well as engages enterprise’s workforce in the development process.
Reward if there’s a cell app. This solution will also accommodate distant personnel and people who travel.
Error code tracking and pattern Evaluation tools deliver visibility of systemic functions and uncover options for continuous quality enhancement.
Conveniently distribute tasks and share accountability inside your Corporation. Empower your staff for being your eyes in the field by doing inspections and audits employing my link their cell or pill unit. click this link Complete digital inspections and right away preserve your information while in the cloud.
It appears to be a small cloud run enterprise out a building with a number of folks which can be great since the products is great but the assistance from profits has Considerably to become desired.
When picking out a provider, Check out the safety safeguards they've in place to shield buyers, including firewalls and encryption.
"Excellent software for chemical Regulate considering excellent manufacturing methods and ISO specifications. It makes it possible for to own the knowledge while in the cloud, updates toward the day-to-working day traits."
Simplify the identification and documentation of new challenges and defects, build new corrective action requests and prioritize requests for corrective motion.
Conveniently generate new compliance modules or import existing content material using our intuitive system builder.
Relevant data from a sort which could perhaps require a corrective action is routinely entered right into a CAPA type, decreasing facts entry and eliminating faults from manually transferring information.
Learn how CAPA Administration has aided this medical product manufacturer do away with CAPA-associated 483s in over two dozen inspections throughout 20 internet sites.
Integration possibilities with other High-quality Programs are furnished, ensuring that there is easy checking