隔离系统与RABS的URS？ 隔离系统与RABS:现代很流行同时也是很安全的A级做法。提供URS User Requirements Template for a BARRIER ISOLATOR AND HVAC SYSTEM REVISION HISTORY Rev. Date Approval Revision Summary A1 11/06/01 T. Petro Draft A2 01/15/02 T. Petro Incorporated content and changes from review by JETT break-out group on 11/15/01. B1 3/1/02 M Casey Validation review C1 11/20/02 M Rivera Format Review C2 11/26/02 T. Petro Final review of content and format by author 0 11/26/02 T. Petro Approved for Initial Release Table of Contents 1.0 Introduction .............................................................................................. 5 2.0 Overview ........................................................................................................ 5 3.0 Operational Requirements ................................................................ 6 3.1 Capacity ......................................................................................................... 6 3.2 Process Requirements ................................................................................. 6 3.3 Process Control .......................................................................................... 6 3.4 Functions ....................................................................................................... 7 3.5 Data and Security ......................................................................................... 9 3.6 Environment ................................................................................................ 11 4.0 Constraints ............................................................................................... 14 4.1 Milestones and Timelines ......................................................................... 14 4.2 Equipment Constraints ............................................................................. 15 4.3 Compatibility and Support ....................................................................... 15 4.4 Availability ................................................................................................. 17 4.5 Procedural Constraints .......................................................................... 17 4.6 Maintenance ................................................................................................ 19 5.0 Life-Cycle ..................................................................................................... 19 5.1 Development ................................................................................................ 19 5.2 Testing .......................................................................................................... 19 5.3 Delivery ........................................................................................................ 20 5.4 Support ......................................................................................................... 21 6.0 Glossary ....................................................................................................... 22 7.0 References .................................................................................................. 23 8.0 Approval ....................................................................................................... 24 Project No.: Insert the unique project number associated with this particular URS. Document No.: Insert the Document Identification Number and Revision. Document Description: Insert description of document, e.g. PURE STEAM GENERATOR, JETT Example User Requirements Specification. 1.0 Introduction Note: Insert your own description and introduction. You may wish to include your own requirements and specifics to allow the inexperienced reader, contractors, and suppliers adequate explanation to understand the scope of the equipment. Describe who produced the document, under what authority, and for what purpose. Describe the contractual status of the document. Include or reference as an attachment the “legal” paragraph that communicates purchasing terms and conditions in this section. Describe the relationship of this document to other documents. This is important for equipment that is part of an integrated process or line and will help the Supplier to understand and ask questions that may otherwise be overlooked. Refer to the Equipment Validation Plan that outlines the Supplier’s responsibilities is attached. Remove any options that are not applicable for this project, if other uses will apply list each separately. This is to be utilized as a guide for the user to answer the majority of questions involved in specifying the “what” for the equipment. Addendums may be used to round out the requirements. 2.0 Overview The Barrier Isolator and HVAC System provides a mechanical separation between the controlled room environment, and the interior environment in which the pharmaceutical product is processed. The barrier isolator is manufactured in such a manner that the materials are resistant to corrosion, do not allow pooling of the cleaning materials, and allow access to the interior as required by the equipment and products. The environment inside the barrier isolator is controlled in a manner to allow the pharmaceutical product to be processed in accordance with the purpose and product requirements. 2.1 USE The equipment shall be used primarily for: · Continuous Production · Batch Production · Other 2.2 EQUIPMENT CLASSIFICATION For example: For providing an aseptic environment for: · Liquid filling of vials with stoppers · Powder filling of vials with stoppers · Liquid filling of ampoules with flame-off · Liquid filling of cartridges with plugs · Liquid filling of syringes · Other (define) Insert your Equipment Classifications here as required using the above example as a guide. 2.3 CLEANING REQUIREMENTS Wipedown Manual Washdown Clean-In-Place (CIP) Special Requirements: – Peracetic Acid – Ethylene Oxide – Chlorine Dioxide – Vaporized Hydrogen Peroxide – Others 2.4 LANGUAGE REQUIREMENTS · English · Other (Specify): ____________________ · Bilingual? Yes / No 3.0 Operational Requirements 3.1 PERFORMANCE REQUIREMENTS 3.1.1 Capacity Add capacities and details concerning equipment capacity here. Identify the type and dimensions of the equipment that will fit inside of the barrier. 3.2 FUNCTIONS The Barrier Isolator and HVAC System is divided into two main portions: The barrier isolator, and the HVAC system. 3.2.1 Barrier Isolator Operation The barrier isolator is an enclosure that provides isolation between the operator/outside environment and the interior of the barrier where the pharmaceutical processing is done. The barrier isolator provides the following functions: · Isolation between the operator and the process · Safety Barrier to separate the operator from equipment hazards · A non-corrosive, drainable, and easily cleaned enclosure. · Doors to provide access to the equipment during cleaning and changeover · Gloveports to allow access to machinery and product during production · Transfer ports to introduce commodities and equipment to the environment · Infeed opening to introduce commodities to the system. · Exit opening to allow finished commodities to exit the system. 3.2.2 Barrier Isolator Design The barrier isolator design will meet current GMP for aseptic product manufacture, along with wash down and sanitization requirements. 1. All interior corners will have a minimum of __ 0.5” _ radius. 2. Drain pans will have a minimum of __ 0.5” __ slope per 12” of run. 3. Horizontal surfaces will be minimized to resist pooling. Pooling of more than __ 5ml __ of liquid is not allowed. Pooled liquid must not be more than __ 2mm __ deep 4. Drain pans shall terminate in tank bottom drain valves with materials and finish equivalent to the rest of the barrier isolator interior. 5. Air distribution from the plenum will use __ dual perforated plates __. 6. The air distribution system will be removable for cleaning. 3.2.2.1 Safety of the operator from the machinery or processes within the barrier isolator must be ensured. 7. All doors will have dual-redundant safety switches that will immediately stop all machinery or processes when the door is opened. 8. Gloveports will be guarded with light curtains to immediately stop machinery. 9. All moving machinery external to the barrier isolator will be fully guarded and alarmed. 10. All high temperature components external to the barrier isolator will be fully guarded and alarmed. 3.2.2.2 Materials and Finish of the Barrier Isolator will meet current GMP’s. 1. Wall thickness of the barrier isolator will be a minimum of __ 7gauge _ Stainless Steel 2. Interior surfaces of the barrier isolator will be manufactured from __ 316L ________ Stainless Steel. 3. Exterior surfaces of the barrier isolator and ductwork will be manufactured from __ 304 or316L ___ Stainless Steel. 4. Interior finish of the barrier isolator will be of _______ 40 _ micro-inch Ra finish maximum. 5. Exterior finish of the barrier isolator will be of ______ 120 _ micro-inch Ra finish maximum. 6. All interior surfaces will be electro-polished redundant? How else do you get #4 and #5?. 7. All welds will be ground and polished to the above finish requirements. 8. Air plenums must meet the same materials and finish requirements as the barrier isolator. 9. The completed interior of the barrier isolator will be passivated prior to shipment to the site. 10. Components attached to the exterior of the barrier isolator must meet current GMP’s and be finished to resist corrosion. 3.2.2.3 Doors and Windows in the barrier isolator allow visibility and access to the interior. 1. The window material is manufactured from __ tempered safety glass or polycarbonate __. 2. The window sealing material is extruded from __ silicone rubber __. 3. Window seals must be designed to prevent pooling. 4. Doors must hinge open to allow access to the interior. 5. Doors must be removable without tools. 3.2.2.4 Mousehole Opening(s) are provided at the exit point to allow the exit of good vials and of reject vials. 1. Mousehole covers are manufactured to the same requirements as the barrier Isolator. 2. Mousehole cover presence is to be sensed and alarmed. 3.2.2.5 Gloveports are provided in the barrier isolator to allow operator access to the interior without compromising sterility. 1. Gloves must be replaceable. 2. Gloves must be sanitized without absorbing sterilant. 3. Gloves will be made from __ fabric reinforced PVC __. 4. Gloves will be located to access common intervention points. 5. Gloves will be positioned to allow access by operators within the normal range of physical sizes. 3.2.2.6 Transfer Ports will be provided to allow component and product entry into the interior of the barrier isolator without compromising sterility. 1. Transfer ports will be located at the following locations, and are of the following sizes: Location #1: ___ upstream of filler __ __ 350mm __ Location #2: ___ at stopper entry ____ __ 270mm __ Location #3: ___ at outfeed ________ __ 270mm __ Location #4: ___ N/A ____________ __________ 2. Transfer port manufacture is _____________________ 3. Transfer port sanitization process is _______________ 3.2.2.7 Commodity/Product Infeed to the interior of the barrier isolator will be provided in the design. 1. Vials enter the barrier isolator from a __ depyrogenation tunnel __. 2. Product enters the barrier isolator through a __ bulkhead fitting __. 3. Stoppers enter the barrier isolator through __ transfer port #2 ____. 4. Miscellaneous Devices such as:__ tools, SMA stands, hangers, platforms, instrumentation, test ports, etc. ___ 3.2.2.8 Product Exit from the interior of the barrier isolator will be provided in the design. 5. Vial path #1 transfers vials to a __flat belt conveyor__. 6. Vial path #2 transfers vials to a __22” transfer disk__. 7. Drains in the bottom of the barrier isolator are provided at __7__ points to allow for liquids to be removed during changeover and sanitization. 8. Drains must be closed during production. 3.2.3 HVAC System Operation The HVAC system controls the environment inside the isolator, and provides the following functions: · Pressure differential between the interior and exterior of the isolator · Temperature control of the interior · Humidity Control of the interior · Air Circulation through the interior · HEPA/ULPA filtration of the interior air · Sanitation of the barrier isolator and the equipment This seems incorrect, it may maintain sanitation but not induce it. 3.2.3.1 Pressure Differential between the interior and exterior is maintained at positive 0.10” H2O , +/- 0.02” H2O . Pressure balance is to be maintained within these parameters under all conditions of: 9. Product infeed doors open or closed 10. Product entering or not entering 11. Exit door open or closed 12. Product exiting or not exiting 13. Multiple withdrawals of glove ports 14. Transition of transfer ports 15. Fluctuation of outside environment within tolerance 3.2.3.2 Temperature Control is maintained at +/- 1.0 ° C of setpoint within the full temperature control range of 5.0 ° C minimum to 50 ° C maximum. Temperature control is to be maintained within these parameters under all conditions of: 1. Beginning of the batch 2. Long term continuous run of the batch 3. Fluctuation of outside environment within tolerance 3.2.3.3 Humidity Control during production is maintained at +/- 1.0 ° C dew point within the full humidity range of 5.0 ° C minimum to 25 ° C maximum. The system is designed to only lower the dew point. There are no provisions to raise the dew point above that of the ambient environment. Humidity control is to be maintained within these parameters under all conditions. 4. Drying of the barrier isolator after cleaning 5. Beginning of the batch 6. Long term continuous run of the batch 7. Fluctuation of outside environment with tolerance 3.2.3.4 Air Circulation is provided by a variable speed fan circulating the air through heating, cooling, dehumidification, and filter systems. The air is forced into the barrier isolator through a perforated plate to disperse the air throughout the interior uniformly. Air is then returned from the interior through the return air ducts. Airflow is measured 12 inches below the perforated plates, and must be between 50 feet per second minimum to 90 feet per second maximum. Air circulation levels are to be maintained within these levels under all conditions. 8. Sanitizing cycle of the barrier isolator 9. Beginning of the batch 10. Long term continuous run of the batch 11. Fluctuation of outside environment with tolerance 3.2.3.5 HEPA/ULPA filtration of the recirculated air is provided by two pairs of filters in series. The filters are 99.99% efficient at removing particles greater than 0.3 microns in size. The fresh air inlet uses a roughing filter and a 90% efficient ASHRAE filter prior to the HEPA/ULPA filters. Recirculated air filtration at all times that the HVAC fan is operating (fragment). 3.2.3.6 Sanitization of the Barrier is provided by the following processes: 12. The interior of the barrier isolator is manually/automatically cleaned out of any debris from the previous production. All areas of the interior that can accumulate debris must be accessible to allow for removal of debris. 13. The interior surfaces of the barrier isolator are able to be wiped down by cleaning personnel easily and efficiently without danger to the personnel or damage to the materials. 14. The interior of the barrier isolator can be washed down with cleaning agents and water without pooling or deterioration of the interior surfaces. 15. The interior surfaces of the barrier isolator are drainable without excessive pooling to allow rapid drying of the interior. 16. Cleaning agents are introduced by injection into the HVAC system through a port in the ductwork after the filters. 17. The interior surfaces of the barrier isolator can be sanitized by _______________ cleaning agents without damage to the surfaces of the barrier isolator. 18. All interior surfaces of the barrier isolator are reached by the sanitization agents. 3.2.4 Power Failure and Recovery On power failure, the system shall fail into a “safe state.” On power restoration, the system shall not restart without operator or communication-link input. Insert your specific power failure / recovery scheme here. For example: In the event of a power failure, the system shall protect in the following priority: · Personnel · Equipment · Product Recovery Methods: Insert your specific recovery scheme here. For example: · Manually re-start based on operator inputs. (Operator initiates power recovery sequence) · Re-start based on last state before loss of power. (System runs through power recovery sequence when operator start signal is given) · If there is an automatic batch reporting system, the information shall be retained in the event of a power failure (A UPS is required for automatic batch reporting systems for data retention). 3.2.5 Emergency Stop Insert your specific E-Stop strategy and communication scheme here. For example: The system shall have an E-Stop system designed to shut down all environmental controls in a safe manner. The E-Stop will be Hard-wired into the filler E-Stop system so that all machinery within the barrier/isolator will stopp immediately upon actuation of any E-Stop button. Determine if the HVAC fan will also stop under an emergency stop. The E-Stop button(s) shall be located in easily accessible areas around the equipment as required by local safety standards. 3.2.6 Alarms And Warnings Insert your Alarm scheme here. For example: 3.2.6.1 “Critical alarms” shall take action automatically to shut the equipment down and notify the operator. The operator shall be required to acknowledge the alarm before the alarm can be reset and the system restarted. Once the alarm is reset, the operator may restart the system. 3.2.6.2 “Non-Critical alarms” shall take action to shut the equipment down at the end of the cycle, and notify the operator once stopped. The operator shall be required to acknowledge the alarm before the alarm can be reset and the system restarted. Once the alarm is reset, the operator may restart the system. 3.2.6.3 “Operator Alert” shall notify the operator and take no further action. Non-Critical warnings and shall sound the alarm horn, illuminate the alarm indicator but allow the system to continue to operate. The operator shall be required to acknowledge the warning in order to silence the alarm horn, and the alarm indicator shall be extinguished when the warning condition disappears. The Equipment shall have the following alarms and warnings: Alarm or Warning Critical Non-Critical Emergency Stop X Control Platform Communication Watchdog X Control Power Fault X Barrier Door Open X Glove Port Light Curtain Interrupted X Mousehole Cover Open X Mousehole Cover Closed X Drain Valve Failed to Open X Drain Valve Failed to Close X Light Curtain Contamination Fault X Recirculation Fan Failed to Start X Filter Differential Pressure Alarm X Barrier High Pressure Alarm X Barrier Low Pressure Alarm X Barrier Differential pressure alarm X PLC Battery Low X Other Alarms as Required 3.3 Data and Security 3.3.1 Interfaces Insert your interface scheme here. For example: The Programmable Logic Controller / Operator-Interface Panel system (hereafter referred to as the “PLC/OIP system”) shall include interfaces with the Operator, Supervisors, external equipment, and the User’s control system to ensure safe, reliable, continuous, and automatic operation and easy, safe, and reliable configuration. This section should address the following issues: - Operator interface access levels - Frequency of data point collection - Hardcopy/electronic data collection requirements - Compliance with 21CFR Part 11 (for Europe - EREC Guidelines) - Data retention time on the system - Data storage media Include the operator interface access levels, e.g. what functions can be access by operators, which only by supervisors, maintenance personnel, etc. - Access to all Input/Output values and system status bits shall be provided through a data-communication link. Security for data and operator access is provided by (Check all that apply): · User ID/Password · Card Reader · Biometric (Fingerprint, eye scan, voice recognition, etc.) 3.3.2 Interface with Supervisors and Operators Insert your interface scheme here. For example: The PLC/OIP system shall include interfaces with the Operator that ensures easy, safe, and reliable operation. An operator-interface panel shall be provided and mounted on the machine. This panel shall provide the necessary switches, indicators, and devices to operate the barrier isolator HVAC system. The following shall be displayed: · System Status (e.g., “state” the system currently is in) · Pressure Differential · Temperature · Humidity · HVAC Fan Speed · Utility Controls · Alarms and Warnings. · Other (specify). Delete any of the listed functions/indications that are not applicable for this application and add additional functions/indications as required. 3.3.2.1 The following shall be accessible only to Supervisors: Security Configurations Control loop variables (i.e., “PID terms”). Ability to force system to a different state. Alarm setpoints. Other ____________ (specify). 3.3.3 Interface with Other Equipment Insert your interface scheme here. Describe, define or give details where possible. For example: Delete any of the listed interfaces that are not applicable for this application and add additional interfaces as required. The control system shall include the interfaces necessary to facilitate operation and configuration. Interface to other equipment may include: · Processing equipment interior to the barrier isolator HVAC system · Commodity infeed systems · Commodity outfeed systems · Exterior HVAC system · Cleaning and sanitization systems · MES or SCADA systems · Others: For example: An RS-232 communications port shall be provided. A Modem communications port shall be provided. A high-speed configuration/monitoring connection shall be provided. 3.3.4 Data Collection · None · Recorder · Process Printout · Electronic process printout, Historical Trending · Electronic process printout, Historical Trending and interface to company network The following shall be recorded: · Differential Pressure · Temperature · Humidity · Pressure Leak Test Rates · Other: ____________________ (Specify) 3.4 ENVIRONMENT In the following section, provide details of the physical environment in which equipment will be operated. 3.4.1 Layout For example: Allocated floor space for the barrier isolator is _______ inches wide by ________ inches in length, with at least a 36 inch corridor around the periphery for the equipment. Vertical clearance is _________ inches. Allocated floor space for the HVAC package is _______ inches by ________ inches with at least a 36 inch corridor around the periphery for the equipment. Vertical clearance is _________ inches. The HVAC package will be: · Mounted directly to the top of the barrier isolator. · Mounted along side (at the same level) as the barrier isolator. · Mounted indirectly above the barrier isolator. · Other See attached drawing #________________________ (if applicable). Note: Layout is specific to the size equipment being used and system requirements of the equipment. 3.4.2 Physical Conditions For Example(s): The barrier isolator and HVAC system will be used for (Check all that apply, insert your equipment requirements here): · Aqueous · Low LEL (Lower Explosion Limit) Solvents · High LEL Solvents · Other Room Classification: · Room will be non-hazardous (Zone 0) · Room will be Class I Div II (Zone 1) (explosive atmosphere present at known times) · Room will be Class I Div I (Zone 2) (explosive atmosphere present at all times) Clean Room Classification: Class A Class B Class C Other Biohazard Level: BL-1 BL-2 Etc. NEMA Rating of enclosures: NEMA 12 (Oil tight) NEMA 4 (Wash down) NEMA 4X (Wash down and non-Corrosive) 3.4.2.1 Intended Operating Environment: The Equipment shall be mounted in a GMP environment with a temperature range of 15 to 25 °C, non-condensing humidity. Vibration levels are: · Negligible · Slight · Severe **smic Zone: · Negligible · Slight · Severe Noise Constraints: (Note: Place in Constraint section) 85 DB from 3 feet EMI / RFI levels are: · Negligible. · Other (specify) _________. The equipment is to be used at the following environmental conditions: Altitude ________ ft above sea level. The following is applicable for HVAC Equipment: Process air enters in from: Indoor Temperature ______ ° C Outdoor Temperature: Minimum: ______ ° C, Maximum: ______ ° C Climatic conditions: Winter dry bulb ______ ° C Winter wet bulb ______ ° C Summer dry bulb _____ ° C Summer wet bulb _____ ° C (If these values are not known, state location to be installed: ) ___________________________________ 3.4.2.2 Containment (move to constraints) 3.4.2.2.1 Explosion Protection Note: This section is only valid if processing products with a risk of explosion. Select one choice. · 2 Bar Construction with isolation and suppression · 10 Bar construction with isolation only · Closed-Loop Nitrogen System 3.4.2.2.2 Containment of Product Note: This section is only valid if the product being used is highly reactive. Insert containment guidelines here. 4.0 Constraints 4.1 Milestones and Timelines Based on the model outlined below, establish the project milestones with a timeline: 4.2 Compatibility and Support Include any requirements for compatibility with other User systems. In the examples provided below, fill in blanks with the appropriate information. Delete areas that are not applicable to this application. 4.2.1 CONTROL PLATFORM Controllers The Supplier shall utilize Control Platform Controllers that shall include a communications port. The Supplier shall provide documentation that the program (embedded software) was developed and coded utilizing program development and documentation software. The supplier shall indicate the use of custom or “bespoke” code within the equipment, and shall supply licensing of the custom code for the life of the equipment. An escrow agreement shall be required in the event the supplier cannot support the supplied custom software any longer. In such instances, the source code and all information regarding the source code shall be given to the user in a timely fashion to prevent downtime of the equipment. 4.2.2 Preferred Vendor List If necessary attach any critical preferred vendors. Refrain from driving the supplier into customizing his equipment package. If the vendor wishes to deviate from the Preferred Instrumentation List, a listing of the proposed components and instrumentation sub-vendors indicating type and model numbers shall be submitted with the quotation, along with an explanation of why the deviation is recommended. 4.2.3 Utilities The utilities and space involved needs to be discussed prior to purchasing the equipment. Obviously, the actual equipment size is but a small part of the entire scope of work necessary to implement a larger system. The unit and its support equipment must be able to be installed in current building facilities. The User shall ensure that the following utilities are available and that the utility supply lines and piping are terminated with fittings or connections, which are compatible with those described on the Customer Connection Drawings. The Supplier shall specify utility data, which is marked with a triangle. Utility data, which are not specified or marked with a triangle, shall be brought to the attention of the User. These data shall be specified (by the User or the Supplier) and shall be approved by both the User and the Supplier before system design begins. Base Utilities Worksheet: Ñ Electricity: ______ VAC ____ Hertz · Single Phase · Three Phase Ñ Uninterruptible Power Supply Required? Yes / No To Power: Entire System / Controls Only Ñ Instrument Air: _______ PSIG (Must be clean, dry ISA instrument quality air, capacity to be determined by size of equipment) Recommend at least 90 PSIG constant air pressure for all equipment unless specified. Ñ Chilled Water: ________ GPH, ________ PSIG, ________ ° C Closed loop with supply and return connections. (can be provided with additives for corrosion resistance if required by the facility, not sanitary) Ñ Fresh Air Inlet: ________ inch diameter air inlet. (can enter from technical area) Temperature of inlet air must be within the same range as required of the machinery. Ñ Exhaust Air: ________ inch diameter air exhaust port. (Provisions must be made for treatment of exhausted air depending on the product and/or sterilant being used in the system.) Ñ Sanitary Water: ________ GPH, _________ PSIG, ________ ° C (Used for wash down (CIP) of the interior of the barrier isolator) Ñ Sterilant: Define the method of sanitization, the delivery system, and the rate sized for the interior volume of the barrier isolator. Not normally supplied as a direct connect utility system. Ñ HVAC Drain: ________ inch diameter (for draining condensate from the cooling coils of the HVAC system) Ñ Barrier Isolator Drain: ________ inch diameter Quantity of _______ drains at various locations throughout the barrier isolator. Tank bottom welded valves that are installed with the same specifications as the tank bottoms (redundant sentence). Ñ Other utility requirements shall be discussed as needed. In the following section, provide details of the physical environment requirements for the system. Items that are listed and that are not applicable should be deleted from the document. Provide additional details as necessary. 4.3 Availability The [ equipment/system ] is intended to be operated [ Continuously, Regularly, __ hours per day, __ hours per week ]. Operation of the [ equipment/system ] shall be suspended, and the system shall be available for preventative maintenance or routine service [ __ hours per week, __ continuous hours per week, __ days per month, __ weeks per year ]. 4.4 Procedural Constraints 4.4.1 Product Contact Materials Describe any local procedural requirements such as local standards, which must be adhered to if applicable. All piping welds and product contact welds shall meet ASME and 3A specification requirements. Product contact metal to be (316L Stainless Steel, 316 Stainless Steel, 304 Stainless Steel, etc.) List critical requirements for surface finish, roughness, etc.. Other standards are attached. The Supplier shall adhere to the indicated sections only. 4.4.2 Product in Contact with Materials All product contact parts should be considered. The [equipment/system] will be used for (aqueous solutions, low LEL (lower explosion limit) solvents, high LEL solvents, etc.). redundant see 3.4.2 What is the difference between this section and 4.4.1? 4.4.3 Noise Level Constraints Insert your own noise level constraint requirements here. For example: The noise level generated during operation of the [ equipment/system ] will not exceed 85 dB from 3 feet away. 4.4.4 EMI / RFI levels are : Insert your own electrical and radio noise immunity requirements here. For example: The [equipment/system] [will/will not] be used in an area where two-way radio communication devices are in operation. The [equipment/system] shall meet CE requirements for electrical noise immunity and emissions. 4.4.5 Containment 4.4.5.1 Explosion Protection This section is only valid if the product being used is highly reactive. Insert containment guidelines here (i.e. Bar Construction with isolation and suppression, 10 Bar construction with isolation only, Closed-Loop Nitrogen System, etc.). 4.4.6 Labeling All equipment and control wiring shall be labeled and identified. 4.5 Maintenance Describe the expected hardware and software maintenance support including: ease of maintenance, expansion capability (software only), likely enhancements (software only), expected lifetime and long-term support. System shall be maintained on a schedule as indicated by the supplier. Supplier is to provide (at minimum) the following maintenance instructions: 1. All sub-systems provided (Maintenance and operation manuals of vendor equipment) 2. A comprehensive lubrication list and recommended lubrication schedule 3. A comprehensive recommended maintenance (regular recommended inspection intervals, wear points, recommended spare parts list) 4. Supplier shall supply ______ Copies of Operation, Installation, Maintenance and de-commissioning manuals 5.0 Life-Cycle 5.1 Development If S88 is to be applied to the equipment being acquired, it should be referenced in this section of the document. The Supplier shall provide a Quality and Project Plan as part of their proposal. The Supplier shall have a quality system in place. Internal quality procedures shall be available for the User’s review. The Supplier shall provide a Project Manager for the project to provide a single communication point with the User. The project shall utilize the GAMP methodology when developing the system and documentation. 5.2 Testing Describe the Supplier testing requirements. Reference the Validation Test Plan, Factory Acceptance Test, special tests, etc. This section should also include required amount of demonstrated run time, any special materials necessary to complete testing, integration testing, etc. In order to verify system performance, the User shall witness the execution of the Factory Acceptance Test procedures. The Supplier shall notify the User _______ weeks in advance of the start of this test. The Factory Acceptance Test Specification shall be submitted to the User for review and approval prior to execution. A minimum of _______ weeks shall be allowed for the User to review and to comment and/or approve the Factory Acceptance Test Specification. Refer to the Equipment Validation Plan for applicable procedures. 5.3 Delivery The [equipment/system], with all options, equipment, and the documentation listed below, shall be delivered to the User’s receiving dock. 5.3.1 Documentation Installation, operation, and maintenance instruction documentation for the system shall be developed to a level that is comprehensible to a high school graduate. The Supplier shall use the formats described in the GAMP Supplier Guide, Current Version, to produce the documentation. The Supplier shall provide the documentation for preliminary review. The Supplier shall provide documentation reflecting “as-built” condition with final delivery. All final documents shall be shipped with transmittals that identify them as contractually required documents. All final documents and drawings shall reflect “as-built” condition. All documents shall in the language of the destination country and supplied with hard copies and electronic versions supplied in the format identified for each document: User should define format for document transmission (ie. MS Word, Autocad, etc.) Below is an example: · Project Plan Microsoft Word 97 (*.doc) · User Requirements Specification Microsoft Word 97 (*.doc) · Functional Specification/Requirements Microsoft Word 97 (*.doc) · Design Specifications Microsoft Word 97 (*.doc) · Controls Test Microsoft Word 97 (*.doc) · Hardware Installation Test Microsoft Word 97 (*.doc) · Operational Test Microsoft Word 97 (*.doc) · Factory Acceptance Test Microsoft Word 97 (*.doc) · Operator, Maintenance and Service Manuals Microsoft Word 97 (*.doc) · Process and Instrumentation Diagram (P&ID) AutoCAD version 12.0 (*.dxf) · Instrument Listing Microsoft Word 97 (*.doc) or Excel 97 (*.xls) · Control Schematics AutoCAD version 12.0 (*.dxf) · Control Panel Assembly Drawings AutoCAD version 12.0 (*.dxf) · Equipment Assembly Drawings AutoCAD version 12.0 (*.dxf) · Bill of Materials Microsoft Word 97 (*.doc) or Excel 97 (*.xls) · Spare Parts List Microsoft Word 97 (*.doc) or Excel 97 (*.xls) · Component Cut Sheets Microsoft Word 97 (*.doc) or Excel 97 (*.xls) · CONTROL PLATFORM Program Printout and Disk File XXX Program Development format · OIP Configuration Printout and Disk File XXX Program Development format 5.4 Support Describe what support activities are required after acceptance. The paragraphs outlined below provide some areas for consideration. 5.4.1 Start-up Support (list available options) 5.4.1.1 Training (list training options available) 5.4.2 Post Start-up Support (list post-startup support available) 5.4.2.1 Technical Support Telephone (Voice or Modem) Replacement Parts Availability List (Normal lead times shall be listed) 5.4.2.2 User Site Support Preventative Maintenance (list maintenance contracts available) System Improvements (supplier shall notify user of any improvements available on a regular basis) 6.0 Glossary If necessary, attach a glossary, which includes definitions of terms that may be unfamiliar to the Supplier or terminology that may have meanings specific to entries on this User Requirements Check sheet. For example ( example list is not intended to be complete ): Acronym Definition ° C Degrees Celsius BL Biohazard Level CFR Code of Federal Regulations dB Decibels EMI Electro-Magnetic Interference ft Feet GUI Graphic User Interface HMI Human – Machine Interface HVAC Heating, Ventilation, and Air Conditioning ISO International Organization for Standardization JETT Joint Equipment Transition Team LEL Lower Explosion Limit OIP Operator Interface Panel RFI Radio Frequency Interference URS User Requirement Specification Table is incomplete 7.0 References List references that were used in preparing this document or that provide additional details, such as: o Equipment Validation Plan o Current revision of GAMP Guidelines o Vendor Piping Certification (if applicable) o Customer Connection Diagram o Approved Instrumentation List o Process Flow Diagram o 21 CFR Part 11 o National Electric Code o S88 8.0 Approval Insert your company’s standard approval page at the appropriate position in the document or utilize the sample approvals listed below. The approval process/requirements should be outlined in the Equipment Validation Plan. This document has been reviewed by the User Project Manager and approved for use by the Supplier. Printed/Typed Name Signature Date This document has been reviewed by the User Quality Assurance Group and approved for use by the Supplier. Printed/Typed Name Signature Date This document has been reviewed by the Supplier Project Manager and approved for use by the Supplier Project Team. Printed/Typed Name Signature Date Other approvals as necessary may be included, such as the Technical Services Groups, User Groups, Engineering, etc. as required. 查看更多0个回答 . 4人已关注
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