Do You Still Want to be a Paper-based Regulated Company?

automated-document-management

Visualize Digital Strategy of Documentation

Pharmaceutical industries deal with diverse types of documents daily. In no time, the pharma companies will be drowned in paper documents if they maintain every little detail in paper. Having a simplified system for document processes is the need of the hour.

  1. Complete paperless approach by digitalization and automation
  2. Configurable document control workflows
  3. Automated compliance with SOPs and GMP standards

Visualize Digital Strategy of Documentation

Pharmaceutical industries deal with diverse types of documents daily. In no time, the pharma companies will be drowned in paper documents if they maintain every little detail in paper. Having a simplified system for document processes is the need of the hour.

  1. Complete paperless approach by digitalization and automation
  2. Configurable document control workflows
  3. Automated compliance with SOPs and GMP standards

Take Control of Document Lifecycle

A document goes through 9 stages before it becomes obsolete or is destroyed. Management of document lifecycle from the initiation stage to storage and finally destruction in a manual paper-based company is difficult. At every stage of document lifecycle, a lot of paperwork, time, effort, and resources get involved.

You can easily control and take charge of the complete documentation lifecycle by using a dynamic document control software like Docs-IQ. The 9 stages of document lifecycle are fully automated leaving no room for transcriptional errors, back-dated entries, direct changes in SOPs, etc.

Take Control of Document Lifecycle

A document goes through 9 stages before it becomes obsolete or is destroyed. Management of document lifecycle from the initiation stage to storage and finally destruction in a manual paper-based company is difficult. At every stage of document lifecycle, a lot of paperwork, time, effort, and resources get involved.

You can easily control and take charge of the complete documentation lifecycle by using a dynamic document control software like Docs-IQ. The 9 stages of document lifecycle are fully automated leaving no room for transcriptional errors, back-dated entries, direct changes in SOPs, etc.

Save Direct & Indirect Operational Costs

Tons of paper logbooks are bought and used every year for all types of logbooks during production. Many people are involved in recording entries and maintenance of record books. A huge amount is spent as storage cost, conveyance charges for for fetching logbooks from storage during audit. Altogether, paper-based documentation is an expensive affair.

Automation of documents is a one-time expense that helps in reducing the direct and indirect operational costs every year. It a win-win situation for companies using Docs-IQ with no paper, personnel, storage, conveyance, and other costs.

Save Direct & Indirect Operational Costs

Tons of paper logbooks are bought and used every year for all types of logbooks during production. Many people are involved in recording entries and maintenance of record books. A huge amount is spent as storage cost, conveyance charges for for fetching logbooks from storage during audit. Altogether, paper-based documentation is an expensive affair.

Automation of documents is a one-time expense that helps in reducing the direct and indirect operational costs every year. It a win-win situation for companies using Docs-IQ with no paper, personnel, storage, conveyance, and other costs.

Go Hand-in-hand with Global Regulations

Utter chaos occurs if there are no proper guidelines for documentation of production process.

In life sciences and other regulated industries documentation is performed following stringent guidelines. Every regulated industry must be compliant to cGMP, ALCOA+, FDA, MHRA, ISO, and many such regulatory bodies’ documentation guidelines. With Docs-IQ, a comprehensive document management solution, you will be able to achieve compliance and data integrity.

Go Hand-in-hand with Global Regulations

Utter chaos occurs if there are no proper guidelines for documentation of production process.

In life sciences and other regulated industries documentation is performed following stringent guidelines. Every regulated industry must be compliant to cGMP, ALCOA+, FDA, MHRA, ISO, and many such regulatory bodies’ documentation guidelines. With Docs-IQ, a comprehensive document management solution, you will be able to achieve compliance and data integrity.

Built for Lifesciences Industry

Flowers

Version Control

Track all the edits and the revisions made in a document. See full information of the changes, users, timestamp, and preserve the original document with version control.

Flowers

Configurable Document Workflow

Align the documentation tasks by easily configuring document workflows. Automate and manage the entire document control process by creating custom flows.

Flowers

Task Prompts

Reduce the document cycle process with timely prompts on approvals, revisions with automated routing and escalation. Get prompts for the next tasks and be proactive.

Flowers

Cross Functional Team Review

Easily communicate and assign tasks for reviews and approvals across teams and departments.

Flowers

Issuance and Retrieval

Automatic system updates and tracking of issuance and retrieval of documents like BPR, BMR in the required formats.

Flowers

Quick Reviews

Do quick at-a-glance reviews by adding and viewing comments on sticky notes. Make swift changes in the document without the actual edits.

Seamless Integration with Other Applications

Sometimes a change or deviation may trigger a change in SOP. In manual paper-based process, it would take much time for the tracking the document, making the changes, completing the review and approval process, training the QA, etc.  It is imperative to choose a document management system that can integrate with other applications, ERP systems to pull data automatically and avoid manual intervention. 

With Docs-IQ and its seamless integration with quality systems and any ERP system, you can trigger a deviation or change request in QMS to make changes in the SOPs directly in the DMS and schedule trainings in CMS. That simple! 

Seamless Integration with Other Applications

Sometimes a change or deviation may trigger a change in SOP. In manual paper-based process, it would take much time for the tracking the document, making the changes, completing the review and approval process, training the QA, etc.  It is imperative to choose a document management system that can integrate with other applications, ERP systems to pull data automatically and avoid manual intervention. 

With Docs-IQ and its seamless integration with quality systems and any ERP system, you can trigger a deviation or change request in QMS to make changes in the SOPs directly in the DMS and schedule trainings in CMS. That simple! 

Trusted by Industry Leaders

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