Wie gebruikt deze software?
Medical device companies looking for an efficient, reliable way to automate and streamline their quality system processes while ensuring regulatory compliance.
Gemiddelde scores
1 review- In totaal 3 / 5
- Gebruiksgemak 3 / 5
- Klantenservice 3 / 5
- Functies 3 / 5
- Waar voor je geld 4 / 5
Productgegevens
- Gratis versie Nee
- Gratis proef Ja
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Implementatie
Cloud, SaaS, Web
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Training
Live online
Documentatie
-
Ondersteuning
Kantooruren
Leveranciergegevens
- Grand Avenue Software
- http://grandavenue.com
- Opgericht in 2002
Over Grand Avenue Software
A modular quality system software suite that helps medical device companies automate their processes and simplify regulatory compliance. Modules include: Audit Management, CAPA, Complaint Handling, Design Control, Document Control, Equipment Management, Nonconforming Materials Reporting, Supplier Management and Training Management. Designed for ISO 13485 and 21 CFR Part 11.
Functies van Grand Avenue Software
- Apparatuurbeheer
- Auditbeheer
- Beheer van ISO-normen
- Compliancebeheer
- Corrigerende en preventieve maatregelen (CAPA)
- Defecten bijhouden
- Documentcontrole
- Klachtenbeheer
- Kwaliteitscontrole van leveranciers
- Onderhoudsbeheer
- Risicobeheer
- Trainingsbeheer
Populaire producten
De nuttigste reviews van Grand Avenue Software
Overall, a good solid basic QMS software
Beoordeeld op 27/7/2017
Rasean H.
Opmerkingen: Allows an early stage medical device company to get off of paper records and into electronic arena. Makes record keeping and trending much easier. No more hunting down a CAPA plan. With Grand Avenue, it's either been completed or it hasn't. No more losing paperwork.
Pluspunten: Most of the modules within Grand Avenue are very easy to use. It is also very easy to print records for an audit.
Minpunten: There is limited flexibility with Grand Avenue (you cannot create additional process flows, only what is offered out of the box). The reporting is also very limited.
Antwoord van de leverancier
van Grand Avenue Software op 11/8/2017
Thanks for the review, Rasean!
The feedback is valid: We've designed our product suite primarily targeting ISO 13485 customers, and each module (e.g. CAPA, Complaint, Document Control, Training, etc.) delivers an out-of-the-box process that is intended to help customers deploy a solution that's easy to validate and keep up-to-date. To accomplish that we've traded some flexibility for a more structured framework that's easier to test and validate each time we release a new version.
Anyway, thanks again for the review/feedback, and we look forward to working with you again in the future.
