BOOST YOUR QMS QUALITY MANAGEMENT SYSTEMS AND MAKE GMP VALIDATIONS FAST & EASY.

VALIDATION PROTOCOL TEMPLATES

ONLINE DOCUMENTS - READY TO USE
  • DOWNLOAD FREE SAMPLES
  • MICROSFT WORD FORMAT
  • HARDCOPY VIA AMAZON

QMS APPLICATION SOFTWARE AS A SERVICE

CSV VALIDATED CLOUD SOLUTION
  • GMP DOCUMENT MANAGEMENT
  • E-SIGNATURE & APPROVALS
  • 21 CFR PART 11 COMPLIANT

Application Features & Modules:

Create, edit and approve all your product review documents.  Keep tracking and follow-up of each pending product review analysis.  Receive notifications and emails when a product review changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your Batch Records or Device History Records.  Keep tracking and follow-up of each planned or pending lot or batch record.  Receive notifications and emails when a batch record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your instigations related to CAPA Corrective and Preventive Actions, etc.  Keep tracking and follow-up of each pending investigation.  Receive notifications and emails when a CAPA changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your cleaning and sanitization records.  Keep tracking and follow-up of each pending cleaning file.  Receive notifications and emails when a cleaning record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your drawings and specifications.  Keep tracking and follow-up of each pending design specification.  Receive notifications and emails when a specification record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your EHS documents.  Keep tracking and follow-up of each pending EHS record.  Receive notifications and emails when an EHS record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your experimental projects.  Keep tracking and follow-up of each pending pilot lot.  Receive notifications and emails when an experimental project changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your FDA submission records.  Keep tracking and follow-up of each submission file.  Receive notifications and emails when a submission record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your media fills studies.  Keep tracking and follow-up of each media fill lot.  Receive notifications and emails when a media fill record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, manage and release all your manufacturing lots.  Keep tracking and follow-up of each planned or pending lots.  Receive notifications and emails when a lot number changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your pest control activities and records.  Keep tracking and follow-up of each pending action.  Receive notifications and emails when a pest control document changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your risk analysis and  FMEA assessments.  Keep tracking and follow-up of each pending risk analysis.  Receive notifications and emails when a risk analysis changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create, edit and approve all your Batch Records or Device History Records.  Keep tracking and follow-up of each planned or pending lot or batch record.  Receive notifications and emails when a batch record changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Create and manage all your training activities and records.  Keep tracking and follow-up of each pending or expired training.  Receive notifications and emails when a training is required or changed it status.  Moreover, you can prepare summary reports and trending graphs customized according to your needs.

Main Benefits:

QUALITY MANAGEMENT PROCEDURE TEMPLATES

ONLINE DOCUMENTS - READY TO USE
  • DOWNLOAD FREE SAMPLES
  • MICROSFT WORD FORMAT
  • HARDCOPY VIA AMAZON

Available SOP Templates:

NEED TECHNICAL SUPPORT ?

Temperature and % Relative Humidity Data loggers.

JOB OPPORTUNITIES

JOIN THE CIQA TEAM!

For experienced professionals, CIQA have different positions with great lerning opportunities. Apply now to start the career of your dreams.

CIQA INTERNSHIP

We have incredible and amazing real work opportunities in your area of expertise for graduated and ungraduated students.

For more information about CIQA Validation Services, Staffing Agency, Datalogger Rental, Office Rent hurricane Proof, Bridal Salon Rent Storm resistance, Office Trailer Rental, Rent Center, Climate Controlled Storage, Kaye Validator 2000 rental and more in Puerto Rico
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