TrackWise Reviews

User friendly, easy to operate

Provide all QMS records in All formats

It's not provide year wise QMS data after downloading short from excel sheet

Trackwise is total paper free system so that we can save environment

I am working in CRO business industry.It is basically Pharmaceutical industry.We have to follow GMP guidelines while manufacturing the product.Trackwise is used to handle the QMS like deviation,change control,CAPA, Audit management,OOS,OOT,Etc.

Everything good in trackwise while using.But multiple users using at the same time,it is getting slow down due to server issue. Remaining everything is fine.It is very useful for our industry.

I am working in CRO business industry.It is basically Pharmaceutical industry.We have to follow GMP guidelines while manufacturing the product.Trackwise is used to handle the QMS like deviation,change control,CAPA, Audit management,OOS,OOT,Etc.

Operation friendly.It was a good experience to use a track wise software. It is very helpfull fo maintain all QMS activity online. I would recommend to use this software.

Nothing dislike in software operation. Good software to be usedfor pharmaceutical sector

To maintain and tracking of QMS activity

TW's user interface, ease of working through this application, it never hangs or gets slow, easy to follow workflows, auto reminders

there is really nothing to be disliked abt TW, its a perfect application for CAPA Deviation Audit records management

It helped me to track my capa deviation audit records, every step has approval steps, with due dates, it flags actions for you, it sends you auto reminders, so even if you are busy with regular tasks you will never miss those actions to be completed in TW. It can also help you with multiple reports as per your requirements.

Trackwise is an easy clear system which is very helpful for quality managing specially for non conformance reporting. This system will save your time and effort for sure.

I have not alot of disadvantages for Trackwise system since this system will be developed, customized and validated before launching. However, some transaction need repeated data which is not necessary.

Non- conformance reports, change control reports and out of specifications as a part of quality system a quality unite in our pharmaceutical manufacturing company.

Tabs at glance with classified information

Sometimes reviewers and approvers are selected who dont have privilages and record gets stuck

Interface have improved over the period of time

Document Management: Allows users to easily create, review, approve, and store documents such as SOPs, policies, and forms.

Corrective and Preventive Action (CAPA): Enables users to efficiently track and resolve issues, prevent recurrences, and improve overall quality processes.

Nonconformance Management: Facilitates the tracking, investigation, and resolution of nonconformance issues.

Audit Management: Allows for the scheduling, execution, and tracking of internal and external audits.

Training Management:

It needs more features. which can help to track easily and effectively.

Document Management: Allows users to easily create, review, approve, and store documents such as SOPs, policies, and forms.

Very easy steps to initiate a incident , deviation, change control and to track all with in one click.

Sometimes it hangs too much , hanging too much slower down process.

This software helps in tracking and collecting data at one click required at the time of audits , so very beneficial in pharmaceutical industry.

It helped in reducing time by ending use of papers in QMS

A bit more clumsy sometimes but can be managed.

Previous to trackwise QMS was paper based but now it is paperless and everything is online

I like trackwise because it arrange all my requirements in one place

Best tool for change control and deviations.

Speed is little slow needs to be improved

Yes I will recommend this to every company who want tot reduce paper work and wants to go for regulatory audits in pharmaceuticals or foods product's.

Change controls deviation risk management

All these things are we manage now easily without wasting paper and it is regulatory accepted.

We have introduced quality incident in trackwise too and that is pretty awesome .

Now it's very easy to handle small incidents in trackwise