Services
Quality Systems Implementation
We can help you implement a new quality system, or help you improve an existing quality system.
A few examples include:
Preparing a list of must-have SOPs and forms, setting up time-frames for completion of these documents, and help with writing the documents.
Preparing document templates so that your documents are standardised.
Help with implementing a document control or training systems.
GMP Gap Assessments
We can come to your site and help you complete a GMP gap assessment so you are confident of where you sit for your next audit.
If you want to do your own gap assessment we can provide you with a gap assessment training. This comes with a free Excel gap assessment template and dashboard, saving you hours of work.
Click here to view details of the Gap Assessment Training Course.
Training
One of our specialties is providing on-site, and off-site GMP, and audit readiness training.
The aim for all training is to make it fun and noteworthy. You spend a lot of money on training, so we want to make sure that the tools we provide will help your staff for years to come.
Current Online Training:
PIC/s GMP Gap Assessment Training
Current On-Site Training:
GMP Training
Root Cause Assessment Training
Customised GMP Training
Audits
Qudos can help you with the following audits:
– Supplier (raw material / packaging material)
– Internal (look at particular areas)
– Mock (a full examination of your systems)
– Documentation (a review of your SOPs)
– External (finished product / laboratory)
Templates
QA personnel spend a lot of time generating or helping others generate documents. We can shave the time, and save you money by providing the following templates and training:
– SOP template with your company logo
– Form template with your company logo
– PIC/s Gap assessment dashboard
– External audit template
– Internal audit template
– Root cause analysis excel template
Technical Writing
We can help you write technical documents that are:
– Written in plain language
– User friendly with photos where applicable
– Plant specific
– PIC/s GMP compliant
Validation
We can help you:
– Write IQ/OQ/PQ/PV Documents
– Perform validation
– Generate a Validation Master Plan
– Generate a Validation Schedule
Quality Inspection and Release
We can inspect and release products, and also examine any complaint samples. This service is especially helpful for those that have only a small number of staff in New Zealand.
