Agenda • Brief Review of Application • Sales tools / literature overview • Instrument – What changed/no? – Consolidated review of the new stuff • Pharmspec – What changed/no? – Consolidated review of new stuff • Best Practice prior to on-site arrival • Review of Inst install (op manual, gotcha’s) • Review of Pharm install (op manual, gotcha’s) • IQ/OQ – brief review • Support team
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Agenda Brief Review of Application Sales tools / literature overview Instrument – What changed/no? – Consolidated review of the new stuff Pharmspec – What.
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Agenda
• Brief Review of Application• Sales tools / literature overview• Instrument – What changed/no?
– Consolidated review of the new stuff• Pharmspec – What changed/no?
– Consolidated review of new stuff• Best Practice prior to on-site arrival• Review of Inst install (op manual, gotcha’s)• Review of Pharm install (op manual, gotcha’s)• IQ/OQ – brief review• Support team
Patent Pending
Literature Resources
Sales Literature• 9703+ Flyer• HIAC Global & Domestic
• Set probe sampling position– Button used to set the pre-configured probe
test sampling position.
Best PracticesCustomer computer (major stumbling block)• Brand new computer• Clean Hard-drive• Recycle• Communication port problems Do you have IQ/OQ documents ready (ideally printed and bound)Brief the customer prior to visit
PharmSpec 3.0Many of the functions
have not changed– Procedural tests– Run Counter tests– IST tests– Procedure Builder – Historical reporting– Activity Log– Data Storage– Hardware settings
What’s New In PharmSpec 3.0• Compatibility with the HIAC 9703+ Liquid Particle Counting System
• Compatibility with MC particle counting sensors
• Users are added to PharmSpec using Windows® User Management
• Users log in to PharmSpec using their Windows user account logins and passwords
• Password expirations and lockout settings are selected using Windows
• USP<789> test procedural standards
• CP test procedural standards
• Procedural standards and user-defined test procedures can be distributed to other computers by the user
What’s New Con’t• Partial results are recorded for incomplete tests
• Automatic checks for procedure and software updates can be scheduled by the user
• Number of reviewer signature lines on printed reports is set by the user
• Company logo can be added to reports by the user
• FDA 21 CFR Part 11 requirement features can be disabled using a license key (logins, user administration, review and approvals of tests, and audit trails)
PharmSpec Requirements*The PC requirements shown are the minimum requirements supported.
*The user may benefit by using a faster processor and/or additional memory.
*Windows Vista and Windows 7 users may have higher requirements.
Bubble Detection Alarm
1) Clear description of alarm
2) Recommended actions
3) Potential cause and where to go for help
Ships disabled as standard.
Adding A User-Right click on “My Computer”
-Click “Manage”
-Double click “Users”
-Next to the “Users” folder, Right click and select “New User”
-The following fields must be filled in: User name, Full name and Password fields. Complete the other fields as needed.
-The following fields must be filled in: User name, Full name and Password fields. Complete the other fields as needed.
Add A User To A Group-Click “Groups”
-Double click on the Group you wish to add the User to. The four groups from which you can choose to add a User to are: 1)PharmSpecAdmins 2) PharmSpecCalTechs 3) PharmSpecOperators 4) PharmSpecSupervisors
- Click Add
-Enter the “User Name” in the dialogue box and click “Check Names”
**If you are working in a Domain and wish to add a Local User click on “Locations” and select your computer.
-Once the User is found select “OK” and the User is added to the selected Group
Included AccesoriesShipping kit1 Nut 7 Probe, small bore2 Hex Key, 1.5 mm 8 Cable, USB3 Syringe, 10 ml 9 Power supply, 24V4 Power cord, AC 10 O-rings5 Stir Bar, Teflon 11 Tubing6 Probe, large bore 12 Power cord, European
HRLD Sensor Install1 2
3 4
HRLD Sensor Install Con’t5
6
7
Instrument Install GuidanceConnect the drain lineThe sample waste from the instrument must be collected in a compatiblewaste container. Monitor the liquid level in the waste container to prevent overflow. Dispose of waste in accordance with local, state and national environmental regulations.
Install the small-vial clampThe optional small-vial clamp connects to the docking module with 2 screws.
Install or remove the docking moduleDocking modules are available for single or multiple-container sampling
Connect the power cordA power supply unit is used to supply power to the instrument
Install Guidance con’tRemove the magnetic stirrerThe magnetic stirrer in the docking module can be removed if
necessary
1. Pull the tab on the docking module away from the instrument to remove the module.
2. Remove the four screws on the bottom plate of the module. Separate the bottom plate from the module enclosure.
3. Pull to remove the stirrer plug from the circuit board.4. Remove the two holding screws from the stirrer motor
flange and remove the magnetic stirrer assembly.5. Put the bottom plate on the module enclosure and install
the four screws.
User interface:The buttons on the front panel allow the user to operate the
syringe, sample probe and stirrer.
1 Syringe controls 4 Stop button2 Stirrer speed (RPM) 5 Sample probe controls3 Power switch 6 LED status indicators
Button Descriptions Button Name Description
Stop Stops the movement of the syringe and probe. Sampling is stopped. The stirrer continues to operate.
Set Moves the sample probe up or down. Hold to increase speed.
Lift/Lower Sends the sample probe to the top or
bottom
IQ/OQ -Validation Support Documentation
Purpose of the Tests The validation project is a set of tests that are used to make sure that the computer-related
system is operating to the specifications that have been identified. Before a full operational qualification (OQ) is done, an installation qualification (IQ) is done.
• On-site IQ/OQ service is available.• IQ/OQ documentation offered to customers as an option
Customer Upgrade - Awareness• We are unable to support PharmSpec 1.X historical database report viewing
– This can be done in PharmSpec versions 1.X and 2.X but not 3.X– PharmSpec 1.X did not migrate to Windows XP, which is the minimum operating system
for PharmSpec 3.0
• All current HRLD sensors in the field must be fitted with the new 9703+ cable when used with new instrument
– Due to speed and sensitivity enhancements, the old HRLD cabling is not optimized for the 9703+
– All new HRLD part #’s with new cable have been developed for quotes on 9703+– Retrofitting the new cable on an old sensor is an acceptable solution
• We no longer user PharmSpec application security, we utilize Windows security for login access
– Be sure to add your user’s to one of the PharmSpec User groups, clearly outlined in the operator manual
Hach Internal 9703+ Support Team• This is an internal list to be used when normal channels of support have not
provided an adequate solution.
Software: Tim Rivas x 6535Software: Guy Wood x 6532Tech Support: John Moir x 6545General Questions: Paul Yates x 6528General Questions: Dave Dunham x 6548
….and when all else failsGary Minnick x 6552Bill Bars x 6551