- Why should you use a Configuration Management Standard such as EIA 649 or Mil-Std-973
- CAPA Procedures - CAPA Program for a Small Pharmaceutical Company
- Source for Quality Assurance Stickers - QC Approved, Reject, Hold, etc.
- When to use an Engineering Change Request (ECR)
- Difference between Control Plan and SOP (Standard Operating Procedure)
- Applying Scanned Signatures to Documents for Signing
- Level 2 Sampling Plan SOP (Standard Operating Procedure) Request
- Process for receiving functions - COTS (commercial off the shelf) vs Custom parts.
- Engineering ECR (Engineering Change Request) and ECN (Eng Change Notice) Procedures
- ISO 9001 - Documentation Control - Letters / Letter Templates
- Customer Charge Back Procedure - Samples and Ideas appreciated!
- Controlling Handler, Tester, Computer and other Equipment Manuals.
- Safety Information Incorporated In Production Records
- Control, Identification and Content of Corporate Electronic Forms
- Change Control - Product Realization example procedure - TS 16949 Clause 7.1.4
- Drawing Control Procedure on Road Construction Project
- Document Control of Internal Auditing Documention
- Identifying and Controlling External Documents
- Looking for stand-alone QMS manual & procedures for ISO 14001 as a guidance document.
- Including individual Quality Objectives in the Quality Manual?
- Correct Document Control - Does each Document need its own Unique Numbering?
- Informal Drawings being Used by Manufacturing
- Document Control in a Construction Management Company
- Effective Dates for Policy and Procedures Manual.
- Including competitors' information in a documentation system
- Part-11 Compliant Document Control & Integrated Training Software
- Analytical Method Transfer Approval and Use
- Procedure for Controlling Transmitted Technical Data - ITAR compliance
- Generate IQ, OQ & PQ (installation/operational/performance qualification) Report
- Form vs. Record - What is the Difference between a Form and a Record
- Procedure for Control of Data, Documented & Electronic needed
- Process Validation of Lathed Products
- Inventory Assessment Procedure (ISO 9001) needed
- HPLC Impurity Method Transfer help needed
- Documentation System Requirements and Document Format procedure - 3.0 Reference
- Structure and Content of DMR / Technical Documentation (FDA vs. ISO 13485)?
- What do you do when a part goes Obsolete and How do you Initiate such a Process?
- Is Electronic Documentation Authorization Acceptable?
- Stockroom Process Procedure example needed
- Approval of Grandfathered Documents - ISO 9000:2000 Clauses 4.2.3 a&b
- Write Quality Manual before Procedures?
- Numbering System for Change Orders used to Manage Controlled Documents
- Technical Documentation, DMR, ISO 13485 vs. FDA, STED
- The Difference between a Document and a Record - Training Plan
- Restructure of Procedures - Need Table of Contents Examples
- Technical File, GHTF's STED and Recommended Content of 510(k) Comparison/Relationship
- How to validate product if gage is determined out of calibration
- Need sample of Control of Document Procedure and Control of External Documents
- Electronic Assembly Test Plan Template
- Does ISO require that documents/procedures have a page/list of revision histories?
- Layout Inspection Format and Improvement
- Hard copies from 10-20 years ago - Document Control and Retention Times question
- Instructions for Use - English into French, German, Italian, Spanish and Swedish
- How to determine the understanding level of QMS documents?
- Archiving Systems to Track Documents - Pharmaceutical Company
- Mock Audit Log Form Template for Product Recall/Return at Food Plant
- Ways where a Document Controller's Effectiveness could be enhanced.
- Process Owners and Process Documentation which Affects Multiple Departments
- How to Control and 'Monitor' External Documents (Documents of External Origin)?
- Gage Out of Tolerance Procedure
- Information or Recommendations for Document Control Software?
- Work Instruction vs. Reference Only document
- Application of Electronic Records & Signatures in Calibration Management Software
- Process Specifications and Control Parameters
- NPI (New Product Introduction) in Electronics Industries
- Microsoft InfoPath - Anyone Ever Used This?
- Small Organizations Document Control and Records - Audit Confusions
- Procurement Cost Saving Report template
- Controlling Reference Material
- Visual Work Instruction examples
- DFT - Demand Flow Technology - Operational Sheets (WI)
- Effective Procedure Implementation Ideas or Suggestions
- Do you control your policies with control numbers?
- Defining Special Characteristics and Control Plan - Welding Operation - Need help
- Engineering Change Request/Order (ECR/ECO) or Document Change Request/Order (DCR/DCO)
- Skill Matrix Format as a Tool to Identify Training Needs
- Control of Non Conforming Process Procedure
- Document Control Management System (MyDMS) & Revision Time Frames
- Exemptions and/or Exclusions from procedures
- Controlling filled out "forms" (eg Operator job specific work instructions)
- Help creating form for shipping w/o MTR's (Material Test Report)
- Is anyone using FormDocs (Electronic Form-Filling Software)?
- Warranty - Is Warranty a Service or not per ISO 9001
- Attaching Labels to Batch Records
- What exactly is a "Process of Record" and what goes into it?
- How to manage standards not under document control
- SAP / EtQ Documentation Systems
- Format for Translation of Controlled Documents into Spanish
- Multi-site, multi-language documentation
- Documentation - Content Management
- Posting of Initials or Names on a Computer Document as Proof of Approval or Task Done
- Live Tracking & Databases - Are they documents or records?
- To ensure that document changes are identified...
- Return Goods Evaluation form
- Item Part Code change - New SAP System
- Stamping Documents that are not being controlled with ‘For Reference Only’
- Making everyone follow documentation (document control) policies
- Definition of Terms in procedures and work instructions
- Control of documents procedure and external documents?
- Templates (Forms) requiring Control - Document Control
- Deviation Form examples
- Combining Separate Document Management Systems
- Any examples of the required ISO Procedures for a small Recruitment Company
- Looking for Rework Form examples
- General Documentation Question-Training Center Process
- Standard Abbreviations for Documentation Identification and Document Prefixes
- Manufacturing Manual - Different type of welding machine
- Difference between Documents and Records? How to control them?
- How to select the requirements for Continuous Sampling Plan (CSP-1&F), Mil-Std 1235C?
- Separate procedures for “identification, collection,..." etc. - ISO 17025 - 4.13.1.1
- Controlled Documents - Trying to differentiate document control levels
- How do you know what documents must be under control?
- Procedure and Annex Revisions - Version number Issue
- Access to, and Printing of, Controlled Documents
- Validation Project Plan example
- Need Help in Writing Procedures
- Mechanical Maintenance Procedures for Oil & Gas wanted
- Is revision level required in the document / form?
- Time and Motion Study Template - Call Center & Business Process Outsourcing Industry
- Should product brochures be controlled per ISO 9001:2000?
- How to document the requirement of clause 4.2.3 (d)
- Are two separate procedures required for Corrective action and preventive actions
- CE Mark Technical Files as controlled document in ISO9001 QMS
- Pipe Supports Visual Examination Procedure example needed
- Too Many purchasing/supplier procedures How do I fix them?
- Drawing Approvals vs. Engineering Order Approvals
- Production Readiness Review Checklist
- Soldering Standard which shows good and bad soldering
- Need a procedure or outline on Good Practices for Completing Quality Records/Document
- BOMs & Test Procedures - Electronic and electro-mechanical systems
- Retention time of quality records for parts with Critical (safety) Characteristics?
- TS 16949 Document (Procedures, etc.) Format Examples/Templates
- DPD (Digital Process Definition)/MBD (Model Based Definition) Procedure
- Acceptance Criteria for Method Transfer for Impurity
- Review of Documents in your Quality System - Frequency of Review
- Contract For Services Template
- What is the best Electronic Document Control Management System?
- Work Instructions Required? Precision metal stamping, cnc machining and wire edm
- Document Control in charge of taking Meeting Minutes?
- Managing ECN (Engineering Change Notice) Blueprints Database..any solutions?
- What companies do a great job at engineering document management systems and control?
- Life Time Quality Record (evidence book) and Quality Plan
- Getting started with ISO 9001:2000 Templates
- Classifying documentation changes for priority
- Sorting Instruction Template wanted
- GP-11 warrant form needed
- Wrong material Ordered - Which Procedure and Form is relevant?
- Layout of the Manual of procedures
- End of Story: Document Abbreviations & Control
- Procedure to Manage, Repair and Modify Tooling needed
- Suspect Material or Quality Issue Form
- IMO our people don't need to read manuals or procedures and document changes to them
- Shipping / Receiving Forklift Truck Work Instruction
- How to handle a company name in order for registration
- Document Control - Internal Departmental battles for control of template
- Are Database Objects Controlled Documents and/or Records?
- Company name in a quality manual
- To what extend should training materials be controlled?
- Four Procedures I need examples of
- Gage Calibration Procedures or Instructions
- Need for revision (minor inconsistencies, missing dates and revision numbers, etc)?
- Inspection Dimensional Check Sheets - Over 500 part numbers
- Procedure for Control of Nonconforming Software Services
- Quality System documents - Can Amendments be made on an 'as and when' basis?
- Question about referencing software - Database Records
- The DREADED...."White Out"!!! *insert scary music*
- Examples of major problems caused by Poor document control
- Batch or Lot release in to market - Need product release procedure
- Certificate statement for Successful Completion of Training
- Document Control Software recommendations for Part 11 medical device
- Shipping Work Instruction needed
- Example of DCR (document change request) form needed
- Should Forms printed for daily use in the shop floor be controlled documents?
- ECR (Engineering Change Request) process - Please critique / review
- Document Control and Agile Product Lifecycle Management software
- Customized EDMS (Electronic Document Management System or ADMS)
- Incoming Materials First Article Inspection (FAI) Procedure needed
- Document Change Notice (DCN) vs. Document Release Notice (DRN) - Differences
- Audit Notification Letter - Sample wanted (Waste contractor audit)
- Inspector Inspection Stamp Requirements and Control Program
- Reproducing parts of a standard in a Procedure - copyright infringement?
- Traceability problems with multiple parts in one lot - Textile Mill
- How to write understandable work instructions
- Document Control Job Description
- VMP template for a Dry Heat Depyrogenation Oven FAT thru PQ
- Building a Database for Equipment Failures
- ISO 9001 Procedures for a University
- Control of various Ink Stamps such as Acceptance, Document Status, etc.
- Critique of Process Flow Diagram
- From ECR (Engineering Change Request) to ECN (Engineering Change Note) - double work!
- Guidance on writing a procedure
- Implementing ISO 9001:2008 - Where to Start?
- Part Naming Convention for SAP ERP Application
- Training needs assessment form wanted
- Control of Label Art, Engineering Drawings, and Documents
- Distribution List of Controlled Documents
- 8 D Report template wanted
- Any CAPA template created due to ISO 9001:2008 requirements?
- How to Control Documents of External Origin
- Stores and Dispatch Training - Multiple choice questions
- 21 CFR part 11 compliant Electronic Document Management Systems
- Obsolete Documents vs. Inactive Documents
- Job title and conformity with the procedure
- Flip Deck for Work Instructions - Flip deck stand that holds 5 x 7 cards wanted
- What to do when form numbers get mixed up on your documents....
- Documentation of training and retraining procedures, specifically how training should
- Setup sheet for machine shop
- How to manage (control) a copy of ISO 9001:2008?
- To change or not to change? Our documents reference ISO 9001:2000
- Various Processes - "Management", "planning" & "feedback", oh my!
- Are environmental compliance documentation quality records?
- Combined Corrective and Preventive Action Procedures?
- When to use a Concession over a Deviation - Concession vs. Deviation
- One company, more plants, different procedures..how to align them ?
- Standard covering all the organization - What standards must I buy?
- Looking for an ECO/ECN logging software
- 93/42/EEC Obsolete Document Retention requirements - New timeframe?
- Departmental Control of Records and Documents
- Who makes archiving decisions in your organization?
- Quality System Manual Revision Control when the manual has sections
- Examples of DCR (Document Change Record) Log and Document Controlled Log
- Master Document List - Is it necessary?
- Approvals for Obsoleting QMS Documents
- Keeping up with all those changes!
- Shutdown Procedure Examples for a chemical manufacturing facility
- Document and Quality Manual Revision Control requirements - Alpha or Numeric
- Procedure for control of Records - Needed
- Evidence required for Document Approval?
- Which kind of document is the Quality Policy?
- Small Precision Parts for Aerospace and Medical Devices - Inspection Procedures
- Information Management vs. Quality Management: New Language Needed!
- Quality Operating Procedures - Eliminating the term 'Quality'
- Tooling Change Request Template
- A good method for referring to an SOP within another SOP
- Is Version Change needed for ammending ISO 9001:2000 to 2008
- Non-conforming product procedure - For a Service Company
- Year-end review checklist for Internal Financial Control
- Specifications - Maintaining current revisions
- Employee Training Database wanted
- How to know how many procedures are too many?
- Total Productive Maintenance Database?
- Reasons for retaining Obsolete Documents and Retention Time
- Electronic Approval Demonstration - Use of the voting option in Outlook
- Return to Stores (RTS) - Examples of a Return to Stores (RTS) form
- Certificate of Compliance-looking for template and have questions
- Simple process for providing Serial/Lot Numbering for our product
- ISO 13485 Documentation Package
- Contamination control required by GM in QSB implementation
- Confusion on declared (part of the quality manual) and non-declared documents
- When to have top level procedure in order to have a work instruction for a process
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