Maximize your efficiency with pdfFiller's comprehensive Document Tracking System for Pharmaceuticals
Boost your daily operations by editing, storing, and tracking documents in one place. With unlimited cloud storage, PDF editing tools, real-time notifications, and audit trails, pdfFiller is the only document management solution you need.
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What makes pdfFiller an outstanding Document Tracking System for Pharmaceuticals?
Explore a vast array of features that enhance the accessibility and traceability of your documents.
End-to-end document workflows
Create documents and fillable forms, gather data and signatures online, and access completed documents in one safe and organized space.
Unlimited cloud storage
Keep your documents and templates safe in a secure cloud accessible from anywhere. Organize files into folders and use smart tags to locate them quickly.
Notifications & audit trails
Receive instant notifications once your documents are completed, reviewed, or edited. Keep track of every action made to your documents or inside your account with audit trails featuring time stamps and IP addresses.
PDF document editor
pdfFiller makes editing, filling out, and annotating PDFs seamless and straightforward. Quickly add text, dates, images, checkboxes, signatures, and other elements to your documents.
Collaboration & versioning
Share documents and templates for review and editing while maintaining control over access permissions. Track document changes and archive previous versions for reference.
Available on mobile
With pdfFiller's mobile apps for iOS and Android, you can access your documents from any device, including laptops, desktop computers, tablets, and smartphones.
Trusted document tracking software
People all over the world use pdfFiller to handle paperwork digitally. Anytime and anywhere.
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users worldwide
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Fortune 500 companies using pdfFiller
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Automate the process of accessing, searching, and editing documents
100% paperless solution
Enhanced productivity & collaboration
Reduced paperwork and labor costs
Why pdfFiller wins
Cloud-native PDF solution
Access pdfFiller from anywhere. No lengthy installation and updates are required.
Top-rated for its ease of use
Edit, share, and track documents with an intuitive UI that only takes minutes to master.
Unlimited document storage
Securely store any number of documents and templates in the cloud.
Unmatched cost-to-value
Benefit from an all-in-one document management solution at a lower price than other brands.
Industry-leading customer service
Enjoy peace of mind with pdfFiller’s highly acclaimed customer support.
Security & compliance
Protect your data according to the highest security standards.
pdfFiller streamlines document management and tracking across industries
Our user reviews speak for themselves
Stay on top of your documents with our Document Tracking System for Pharmaceuticals
Lost files, safety issues, restricted storage capacity, and inefficient document workflows - sound all too familiar in the Pharmaceuticals sector? Using Document Tracking System that can also be leveraged as a collaboration platform could make a world of difference to your company. These online production features ultimately function like a “document assembly line” that moves your paperwork via your company’s teams, enabling each to enhance value and precision that perfects your final product.
With pdfFiller, our custom-made Document Tracking System for Pharmaceuticals, you’ll get all you need to transform inefficiencies and roadblocks into more structured and orderly document-driven processes. pdfFiller brings together document management, eSigning, data collection, document execution, and so much more under one roof. Let’s take a closer look at what it provides.
How pdfFiller can improve your document-based workflows
01
Go paperless: Declutter your physical storage spaces by moving and saving, and managing all your paperwork online in the cloud.
02
Enhance your security: Control challenges induced by dispersed documentation - centralize your data in one safe platform.
03
Streamline adherence: Use our Document Tracking System for Pharmaceuticals to handle your files safely, following field-adherent rules.
04
Supercharge team collaboration: Supply your team with features that foster productivity and improve workflows.
05
Gain a centralized hub for your documents: Keep, access, and audit documents with ease, all from one safe location.
06
Leverage a powerhouse of document-centric features: From document generation and editing to automated eSigning and automated document routing - get everything you need to get rid of the routine from your routine operations.
Use our Document Tracking System for Pharmaceuticals to boost how you handle, store, and work together on paperwork. Turn your organization into a more efficient, safe, and cooperative environment. Stay ahead of your competitors - start examining our dynamic tracking and collaboration set of tools today!
Ready to get started?
Jump in and try our Document Tracking System for Pharmaceuticals hands-on!
Store and organize documents
Edit PDFs on the go and collaborate
Track documents and their versions
Questions & answers
Below is a list of the most common customer questions.
If you can’t find an answer to your question, please don’t hesitate to reach out to us.
What is a document management system in pharma?
Electronic Document Management. The software provides a centralized platform for managing all types of documents related to drug development, production, and regulatory compliance. This includes batch records, SOPs, clinical trial protocols, regulatory submissions, and more. Version Control and Revision Management.
What is document control in pharmaceutical industry?
Pharmaceuticals Pharmaceutical companies must adhere to strict regulations and maintain comprehensive documentation throughout drug development, clinical trials, and production processes. A document control system helps manage and track these critical documents efficiently.
What is documentation work in the pharmaceutical industry?
Documentation is an essential part of good manufacturing practices in the pharmaceutical industry. Key aspects of documentation include master production records, batch records, material identification systems, laboratory records, distribution records, and complaint files. Documentation in Pharmaceutical Industry | PPT - SlideShare SlideShare slideshow documentation-i SlideShare slideshow documentation-i
How to review documents in the pharmaceutical industry?
Verify that documents adhere to applicable regulations, guidelines, and internal policies. Assess if the documents reflect current industry best practices and comply with relevant quality standards (e.g., Good Manufacturing Practices, Good Documentation Practices). Document maintenance in pharmaceutical industry CUTM Courseware uploads 2021/03 Doc CUTM Courseware uploads 2021/03 Doc
What are good documentation practices in pharma?
Good Documentation Practices (GDP) is a term used by the pharmaceutical, laboratory and manufacturing industries to describe best practices surrounding the creation and maintenance of documentation (in both paper and electronic format). Good Documentation Practices (GDP) - Office for Human Subject Protection University of Rochester ohsp study-documentation University of Rochester ohsp study-documentation
What is document management system in pharmaceutical industry?
Pharmaceutical document management can be defined as a system that captures, stores, and tracks all the documents related to the development, production, and distribution of pharmaceutical products. It can be considered one of the most critical components of your organization's pharmaceutical quality management system. A Guide to Effective Pharmaceutical Document Management SimplerQMS Document Control SimplerQMS Document Control
What is eDMS system in pharma?
eDMS helps to ensure product quality in pharmaceutical manufacturing by providing a centralized repository for managing product specifications, batch records, and other quality-related documents.
How is documentation done in pharmaceutical industry?
Documentation is an essential part of good manufacturing practices in the pharmaceutical industry. Key aspects of documentation include master production records, batch records, material identification systems, laboratory records, distribution records, and complaint files.