Pricing

Transparent price plans for you to stay on top of the game and remain competitive.

Now you can enjoy staying compliant.

Billing Frequency

• Monthly
• Yearly

Smart Document Generator

SGD 0/month

Try For Free

Starter

SGD 350/month

Try For Free

Professional (Most Popular)

SGD 1000/month

Try For Free

Enterprise

Talk to us!

Try For Free

Smart Document Generator

SGD 0/year

Try For Free

Starter

SGD 3500/year

Try For Free

Professional (Most Popular)

SGD 10000/year

Try For Free

Enterprise

Talk to us!

Try For Free

Features

Smart Document Generator

Starter

Professional

Enterprise

Number of Users

2 Users

5 Users

10 Users

Recommended for team size 50+ people

Features

Free Plan

Starter

Pro.

Ent.

User

2

5

10

30+

Storage Capacity

30 GB Can't be extended

100 GB Can be extended

500 GB Can be extended

View features comparison

Document Generator

The document generator in Stendard Solution™ uses a simple Question and Answer (Q&A) engine to decide, permutate and recommend a list of documentation based on your industry, type of business and standard requirement.

As such, different document combination (Quality Manual, Standard Operating Procedure and Form) is applicable to different organisation and would therefore range differently in prices.

To find out the exact price tag for generating customised documents, sign up for an account in Solution™, answer the simple survey and pick the document that you would like to own.

The following price range is an estimate for each document from standard:

Medical Device: ISO 13485 (incl. ISO 14971, IEC 62304, EU MDR/IVDR and US FDA 21 CFR Part 820)

• Quality Manual
  • Organisation Chart
  • QMS Process Interaction Diagram
  • Quality Policy & Objectives
  • Product Master List
• Control of Documents Procedure
  • Standard Operating Procedure Template
  • Work Instruction Template
  • Document and Record Control Plan
• Control of Records Procedure
  • Minutes of Meeting
• Good Documentation Practice Procedure
• Management Review Procedure
  • Minutes of Management Review
• Competency and Training Procedure
  • Job Description
  • Employee Competency Matrix
  • Annual Training Program
  • Training Evaluation Form
• Maintenance of Infrastructure Procedure
  • Software Infrastructure List
  • Equipment Master List and Maintenance Programme
  • Preventive Maintenance Form
  • Calibration Verification Form
  • Corrective Maintenance (Repair) Form
  • Qualification Status Label
  • Calibration Status Label
  • Red Tag Label
  • Machine Cleanliness Label
• Maintenance of Work Environment Procedure
  • Pest Control Plan
  • Pest Monitoring Form
  • Room Cleanliness Checklist
  • Temperature and Humidity Monitoring Form
• Design and Development Procedure
  • Design and Development Plan
  • Design Control Traceability Matrix
  • Product Specification
  • Design and Development Files (Design History File)
  • Design Transfer Checklist
• Software Design and Development Procedure
  • Software Design and Development Plan
  • Software Design Control Traceability Matrix
  • Software Requirement Specification
  • Software Architectural and Detailed Design
  • Software Design and Development Files (Design History File)
• Software Release and Maintenance Procedure
  • Software Product Release Checklist
• Software Configuration Management Procedure
• Change Control Procedure
  • Change Request Form
  • Change Closure Form
• Risk Management Procedure
  • Risk Management Plan
  • Failure Mode Effect Analysis
  • Risk Management Report
• Supplier Management Procedure
  • Supplier Evaluation Questionnaire
  • Supplier Evaluation Report
  • Approved Supplier List
  • Supplier Performance Report
  • Agreement
• Purchasing Procedure
  • Purchase Request Form
  • Purchase Order
  • Goods Received Note
  • Goods Return Note
• Inventory Control Procedure
  • Material Master List
  • Product/Material Inventory Control
• Production Planning Procedure
  • Work Order
  • Material Issue
• Production Control Procedure
  • Production Process Flowchart
  • Production Control Plan and Record
  • Quality Control Form
  • Material/Component Specification
  • Artwork/Drawing Specification
  • Bill of Material
• Qualification, Verification and Validation Procedure
  • Protocol Form
  • Report Form
  • Validation Master Plan
  • User Requirements Specification
• Product Release Procedure
  • Product Release Checklist
  • Certificate of Conformance
• Traceability and Identification Procedure
  • Quarantined Status Label
  • Work In Process Status Label
  • Released Status Label
  • Rejected Status Label
• Sales Procedure
  • Sales Quotation
• Distribution Management Procedure
  • Delivery Order
  • Packing List
  • Outgoing Inspection Report
  • Distributor Evaluation Questionnaire
• Installation Procedure
  • Installation Record
• Servicing Procedure
  • Servicing Record
• Analysis of Data Procedure
• Feedback and Complaint Management Procedure
  • Customer Satisfaction Survey Form
  • Customer Feedback and Complaint Form
• Adverse Event Reporting Procedure
• Field Safety Corrective Action (FSCA) Reporting Procedure
• Product Recall Procedure
  • Recall Report Form
• Audit Programme Procedure
  • Annual Audit Schedule
  • Audit Checklist
  • Audit Plan
  • Audit Report
• Nonconformity Handling Procedure
  • Nonconformity Report
  • Nonconformity Investigation Report
• Corrective Action and Preventive Action Procedure
  • CAPA Tracking
• Medical Device File Procedure
  • Medical Device File
• Technical Documentation Procedure
  • Technical Dossier (Singapore CSDT non-IVD)
  • Technical Dossier (Singapore CSDT IVD)
  • Singapore Essential Principles Conformity Checklist
  • Technical Documentation (MDR)
  • Technical Documentation (IVDR)
  • General Safety and Performance Requirements Checklist (MDR)
  • General Safety and Performance Requirements Checklist (IVDR)
  • EU Declaration of Conformity
• Clinical Evaluation Procedure (Non-IVD)
  • Clinical Evaluation Report
• Post-Market Surveillance Procedure
  • PMS Plan
  • PMS Report
  • Periodic and Safety Update Report (PSUR)
  • PMCF / PMPF Evaluation Report
  • Summary of Safety and Clinical Performance (SSCP)
• Performance Evaluation Procedure (IVDs)
  • Performance Evaluation Report

SGD 1088

Information Security Management System : ISO 27001

List of ISO 27001 documents

• Information Security Manual

• Control of Documents Procedure

• Standard Operating Procedure Template

  • Work Instruction Template
  • Document and Record Control Plan

• Control of Records Procedure

• Minutes of Meeting

• Good Documentation Practice Procedure

• Management Review Procedure

• Minutes of Management Review

• Competency and Training Procedure

• Job Description

  • Employee Competency Matrix
  • Annual Training Program
  • Training Evaluation Form
  • Procedural Competency Matrix

• Maintenance of Infrastructure Procedure

• Software Infrastructure List

• Change Control Procedure

• Change Request Form

  • Change Closure Form

• Risk Management Procedure

  • Information Security Risk Management Form
  • Threat Intelligence Analysis Form

• Purchasing Procedure

• Purchase Request Form

  • Purchase Order

• Qualification, Verification and Validation Procedure

• Protocol Form

  • Report Form
  • User Requirements Specification

• Feedback and Complaint Management Procedure

• Customer Feedback and Complaint Form

• Audit Programme Procedure

  • Annual Audit Schedule
  • Audit Checklist (ISO 27001)
  • Audit Plan
  • Audit Report

• Corrective Action of Nonconformance Procedure

  • Nonconformity Report
  • Corrective Action Tracking Log

• Acceptable Use of Assets Procedure

• Software Design and Development Procedure

• Software Design Control Traceability Matrix

• Information Transfer Procedure

• Mobile Device and Teleworking Procedure

• Password Management Procedure

• Clear Desk and Clear Screen Procedure

• Bring Your Own Device Procedure

  • Personally-Owned Device User List Form
  • Blacklist Applications Form
  • Allowable Device Form

• Access Control Procedure

  • Access Right User Profile Form
  • Access Right Request Form
  • Access Right Review Form

• Data Backup Procedure

• Capacity Management Procedure

  • Year-End Prediction Analysis Form
  • Capacity Analysis Form

• Identification of Regulations and Other Requirements Procedure

  • Identification of Regulations and Other Requirements Form

• Employee Recruitment Procedure

  • Employment Contract
  • Employee Exit Clearance Form
  • Background Verification Form
  • Authorisation of Background Verification

• Information Security Incident Procedure

  • ISIRT Activation Form
  • Information Security Incident Log Form
  • Information Security Incident Handling Report Form
  • Information Security Incident Eradication Form
  • Information Security Incident Containment Form

• Information Classification Procedure

  • Asset Register Form

• Information and Communication Technology Procedure

• Cryptographic Control and Data Masking Procedure

  • Cryptographic Control Form

• Disposal and Destruction Procedure

  • Log of Information Asset Disposal and Destruction Form

• Disaster Recovery Plan Procedure

  • Key Personnel Form
  • Emergency Contact List Form
  • Disaster Recovery Event Recording Form
  • Monitoring Business Recovery Task Progress Form
  • Communications Form
  • Tabletop Exercise Form

• Cloud Security Procedure

• Supplier Management Procedure

  • Supplier Evaluation Questionnaire
  • Supplier Evaluation Report
  • Approved Supplier List
  • Supplier Performance Report
  • Agreement

SGD 958

Food Safety: ISO 22000

List of ISO 22000 documents

• FSMS Manual
• Context of Organisation SOP
  • Interested Parties Requirement Form
  • Issues Log Form
• Risk Management SOP
  • Opportunity Register Form
  • Risk and Opportunity Management Plan
  • Risk Register Form
• Change Management SOP
  • Change Control Request Form Part I
  • Change Control Request Form Part II
• Internal and External Communication SOP
  • Communication Plan Form
• Traceability System SOP
  • Material Inventory Log
  • Product Inventory Log
• Emergency Preparedness and Response SOP
  • Emergency Response Plan Form
  • Emergency Situation Reporting Form
• Control of Documents SOP
  • Business Process Flow Diagram Form
  • Organisation Chart Form
  • Schematic Floor Plan Form
  • Food Safety Policy and Objectives Form
• Control of Records SOP
• Internal Audit SOP
  • Internal Audit Checklist Form
  • Internal Audit Programme Form
• Management Review SOP
  • Minutes of Meeting Form
• Corrective Action of Non-conformance SOP
  • NC Investigation Form
  • NC Evaluation Form
• Feedback and Complaint Handling SOP
• Competency and Training SOP
  • Annual Training Plan Form
  • Employee Training Effectiveness Form
  • Employee Training Form
  • Job Description Form
• Pre-requisite Programme SOP
  • PRP Identification and Evaluation Form
• HACCP SOP
  • HACCP Plan Form
  • Hazard Analysis Form
  • OPRP Plan Form
  • Product Information Form
• Maintenance and Calibration SOP
  • Equipment List Form
  • Maintenance Instruction Form
• Purchasing and Supplier Selection SOP
  • Goods Return Form
  • Purchase Order Form
  • Receiving Inspection Form
  • Supplier Evaluation Form
  • Supplier List Form
  • Supplier Re-evaluation Form
• Testing and Inspection SOP
  • List of Test Results Form
  • Operational Inspection Checklist Form

SGD 958

General: ISO 9001

List of ISO 9001 documents

• Quality Manual
• Context of Organisation SOP
  • Issues Log Form
  • Interested Parties Requirement Form
• Risk Management SOP
  • Risk and Opportunity Management Plan
  • Risk Register Form
  • Opportunity Register Form
• Change Management SOP
  • Change Control Request Form Part I
  • Change Control Request Form Part II
• Internal and External Communication SOP
  • Communication Plan Form
• Traceability System SOP
  • Material Inventory Log
  • Product Inventory Log
  • Service Traceability Form
• Control of Documents SOP
  • Business Process Flow Diagram Form
  • Quality Policy and Objectives Form
  • Organisation Chart Form
  • Schematic Floor Plan Form
• Control of Records SOP
• Internal Audit SOP
  • Internal Audit Programme Form
  • Internal Audit Checklist Form
• Management Review SOP
  • Minutes of Meeting Form
• Corrective Action of Nonconformance SOP
  • NC Investigation Form
  • NC Evaluation Form
• Feedback and Complaint Handling SOP
  • Customer Survey Form
• Competency and Training SOP
  • Annual Training Plan Form
  • Employee Training Form
  • Employee Training Effectiveness Form
  • Job Description Form
• Maintenance and Calibration SOP
  • Equipment List Form
  • Maintenance Instruction Form
• Purchasing and Supplier Selection SOP
  • Goods Return Form
  • Purchase Order Form
  • Receiving Inspection Form
  • Supplier Evaluation Form
  • Supplier List Form
  • Supplier Re-evaluation Form
• Testing and Inspection SOP
  • List of Test Results Form
  • Operational Inspection Checklist Form
• Operational Planning and Control SOP
  • Quality Plan Form
  • Quality Review Checklist Form
• Design and Development SOP
  • Design & Development Plan
  • Traceability Matrix Form
  • Design & Development Review Checklist
  • Design & Development History File
• Customer and External Provider Property SOP
• Sales Execution SOP
  • Sales Quotation
  • Sales Invoice
  • Delivery Order
• Work Instruction Template

SGD 818

Food Safety: SS 444

List of SS 444 documents

• HACCP Manual
• Control of Documents SOP
  • Business Process Flow Diagram Form
  • Organisation Chart Form
  • Schematic Floor Plan Form
  • Food Safety Policy and Objective Form
• Control of Records SOP
• Competency and Training SOP
  • Annual Training Plan Form
  • Employee Training Effectiveness Form
  • Employee Training Form
  • Job Description Form
• Corrective Action of Non-conformance SOP
  • NC Investigation Form
  • NC Evaluation Form
• Feedback and Complaint Handling SOP
• HACCP SOP
  • HACCP Plan Form
  • Hazard Analysis Form
  • Product Information Form
• Internal Audit SOP
  • Internal Audit Checklist
  • Internal Audit Programme Form
• Maintenance and Calibration SOP
  • Equipment List Form
  • Maintenance Instruction Form
• Management Review SOP
  • Minutes of Meeting Form
• Pre-requisite Programme SOP
  • PRP Identification and Evaluation Form
• Purchasing and Supplier Selection SOP
  • Goods Return Form
  • Purchase Order Form
  • Receiving Inspection Form
  • Supplier Evaluation Form
  • Supplier List Form
  • Supplier Re-evaluation Form
• Testing and Inspection SOP
  • List of Test Results Form
  • Operational Inspection Checklist Form
• Work Instruction Template

SGD 818

Medical Device: SS 620

List of SS 620 documents

• Site Master File
• Control of Documents SOP
• Control of Records SOP
  • Minutes of Meeting Form
• Management Review SOP
• Competency and Training SOP
  • Job Description Form
  • Employee Training Effectiveness Form
  • Employee Training Form
  • Annual Training Plan Form
• Storage and Stock Handling SOP
  • Receiving Inspection Form
  • Inventory Log Form
  • Cleanliness Maintenance Form
  • Pest Control Form
• Control of Non-Conforming Product SOP
  • NC Investigation Form
  • NC Evaluation Form
• Corrective and Preventive Action SOP
• Secondary Assembly SOP
  • Product Assembly Log
• Feedback and Complaint Handling SOP
• Adverse Event Reporting SOP
• Field Safety Corrective Action (FSCA) Reporting SOP
• Internal Audit SOP
  • Supplier Evaluation Form
  • Internal Audit Schedule Form
  • Internal Audit Checklist
• Work Instruction Template

SGD 818

Consultancy and other miscellaneous cost

We understand that not every client require the exact item outside of the above items that are all software related.

We also provide offline services that would be able to give all our clients like yourself a better one-stop services. It may include, but not limited to, the following:

Training

• Customised corporate training programme
• Mass licenses for attending Stendard Academy courses
• Organisation gap analysis

Mock audit / Internal audit

Consultancy

• Product Strategy Planning
• Product Development

Software Validation

• Production & Manufacturing
• Product Registration / License Holder

Quality Management System

• In-depth document customisation
• Document reviewing

Integrated Quality Management System

• EU MDR Inclusion

Don’t see what you would need from this list?

Request for it now!

Do you have any questions?

Drop us an inquiry now!

Get In Touch