Software for Electronic Documents

T

tomjess

#1
electronic format

Does anyone know of any software that I can buy to do the companies manual on.

Thanks in advance
 
Elsmar Forum Sponsor

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#2
Something Special?

There are a lot of threads here in the forums on electronic documentation. The easiest is to just use Word. Everyone has it. Is there something special you're trying to do? :thedeal:
 

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#3
Depends upon the company size, document purpose, etc., but if all tomjess wants to do is write the manual there's probably no need for all the fancy stuff.
 
A

Atul Khandekar

#4
I would agree with Jim Wade. Using MS Office or Lotus Notes with hyperlinking is probably the easiest way to go. Only you will have to be careful about security issues ( authorized access etc.) You'll find this issue discussed in the other threads that Marc has referred to.

If you do a search for 'Quality Manuals' on the web, you could get a whole lot of sites offering readymade templates (I am not sure if this should be recommended !) that could be modified to suit your needs.
 
Thread starter Similar threads Forum Replies Date
J Control of Electronic Forms and Documents Embedded in Software Document Control Systems, Procedures, Forms and Templates 12
T Electronic ECO/ECR Process - Software recommendations Document Control Systems, Procedures, Forms and Templates 3
D Benefits of electronic QMS software Software Quality Assurance 5
G Looking to move to an electronic QMS software Software Quality Assurance 11
M Suggestions for Electronic Signature Software (FDA 21 CFR Part 11 Compliant) Qualification and Validation (including 21 CFR Part 11) 12
I How much does an eQMS (Electronic/Software QMS) cost? Quality Assurance and Compliance Software Tools and Solutions 1
J Electronic Device History Record (eDHR) Software Recommendations 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
D Electronic Logbook Software - 21 CFR part 211 environment (CFR 211.182) Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 6
R A simple electronic (software) document control question ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
H Involving into Electronic and Software Design Issues Quality Manager and Management Related Issues 3
R Moving to an Electronic System - Quality System Software Recommendations ISO 13485:2016 - Medical Device Quality Management Systems 5
C Process Mapping Electronic Document Control Software Recommendations Quality Tools, Improvement and Analysis 5
V Electronic Document Control Software suggestions wanted Document Control Systems, Procedures, Forms and Templates 14
D Electronic Paperless Documentation Software Discussion Document Control Systems, Procedures, Forms and Templates 10
T Electronic Records and Software Development ISO 13485:2016 - Medical Device Quality Management Systems 7
F Looking for Electronic Document Control Software Quality Assurance and Compliance Software Tools and Solutions 14
J Calibrating Electronic Equipment Tester Software - ISO 9001 Clause 7.6 Benchmarking 1
Q Is anyone using FormDocs (Electronic Form-Filling Software)? Document Control Systems, Procedures, Forms and Templates 12
K Application of Electronic Records & Signatures in Calibration Management Software Document Control Systems, Procedures, Forms and Templates 0
C Electronic work instructions - recommendations for electronic data control software. Document Control Systems, Procedures, Forms and Templates 3
R Moving all of our SPC charts to an Electronic System - Software to flag OOC Condition Statistical Analysis Tools, Techniques and SPC 7
A What Electronic Document Control Software are you using? 'Canned' or In-House? Document Control Systems, Procedures, Forms and Templates 10
J Electronic Document and Records Control Software Records and Data - Quality, Legal and Other Evidence 28
B Electronic Doc Control Software Packages Document Control Systems, Procedures, Forms and Templates 3
M Paperless Electronic Document and Records Systems Software Records and Data - Quality, Legal and Other Evidence 19
Q Software as a medical device vs software not sold as medical device: local regulations for sale? EU Medical Device Regulations 4
Y Software updates considered servicing (7.5.4) ISO 13485:2016 - Medical Device Quality Management Systems 4
S How to perform verification of the Statistical Analysis Software? Qualification and Validation (including 21 CFR Part 11) 2
I Document Control Software Document Control Systems, Procedures, Forms and Templates 2
E Software maintenance Process Software maintenance Process to IEC 6204? IEC 62304 - Medical Device Software Life Cycle Processes 3
L Micro-Vu InSpec Software Program Qualification and Validation (including 21 CFR Part 11) 6
A For software change - New Channel of interoperability CE Marking (Conformité Européene) / CB Scheme 4
T IVDR Medical device software CE Marking (Conformité Européene) / CB Scheme 8
N ISO 13485 7.3.9 Change control in medical device software ISO 13485:2016 - Medical Device Quality Management Systems 6
C SharePoint Contract Management Software General Information Resources 0
gramps What do you think about automated QA testing For software app industry? Misc. Quality Assurance and Business Systems Related Topics 5
V Software as medical device (SaMD) replicated for multiple clients through APIs IEC 62304 - Medical Device Software Life Cycle Processes 5
U API Spec Q1 - 5.6.1.2 C (3) - Design software Oil and Gas Industry Standards and Regulations 3
B Complaint Records - Accessing records on Easy Track Software Records and Data - Quality, Legal and Other Evidence 3
GreatNate Master Control QMS software Quality Tools, Improvement and Analysis 0
GreatNate Anyone using the Intellect QMS software? Quality Assurance and Compliance Software Tools and Solutions 1
S DHF/DMR/MDF for a software-only, cloud-based, single-instance device Medical Information Technology, Medical Software and Health Informatics 2
H Software Validation for FFS Packaging Machine Qualification and Validation (including 21 CFR Part 11) 1
E Any sample of a full software life cycle IEC 62304 report ( any class )? IEC 62304 - Medical Device Software Life Cycle Processes 1
Q ISO 13485 7.5.6 Validation - Off the shelf Software ISO 13485:2016 - Medical Device Quality Management Systems 3
M ERP / QMS related software standards for Validation IEC 62304 - Medical Device Software Life Cycle Processes 6
J Do Software Subcontractors need to be ISO13485 compliant in the EU? EU Medical Device Regulations 3
D Safety data sheets software REACH and RoHS Conversations 2
N What are the software audit and control steps Reliability Analysis - Predictions, Testing and Standards 2
N Validating Software before getting approved as Class 2 device US Food and Drug Administration (FDA) 5

Similar threads

Top Bottom