SBS - The best value in QMS software

Issues with REES Environmental Monitoring System

#1
I work for a pharma that uses REES Environmental Monitoring System to monitor the entire facility. REES monitors the temperature, humidity, and differential pressure all across the facility. I have worked with this software at my previous job as well and it still has the same issues such as Inputs dropping, losing connectivity, battery drainage...

Has anyone used this software and was able to "tame the beast?" Or does anyone deal with other issues that you can make me aware of? I am trying to address all of the issues and hopefully have this system working to the point where there never are any of these issues.

Please help!
 
Elsmar Forum Sponsor

sreekiran14

Starting to get Involved
#2
Hi, our company uses Rees but I never used it and this is useful information as I am planning to validate the system.

Do you happened to know if it is validated for Part 11 Compliance in your organization?

Thank you
 
Thread starter Similar threads Forum Replies Date
A OQ and reporting issues Qualification and Validation (including 21 CFR Part 11) 2
A OEM On-Site Calibration issues during Covid19 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
G Issues/Roadblocks with APQP implementation APQP and PPAP 7
G Resistance to solve Issues Customer Complaints 8
G Engineering retest in line - Machine stability issues IATF 16949 - Automotive Quality Systems Standard 8
F Issues in Uncertainty Estimation Measurement Uncertainty (MU) 5
R Robotic weld cell - maintenance issues - expertise needed Manufacturing and Related Processes 0
K Implant Card - Full Manufacturer's Address - Space issues EU Medical Device Regulations 4
A Labeling - 2017/745 - EUMDR Requirements and Trademark Issues EU Medical Device Regulations 0
Q Connecting AS9100 D Clause 4.2 to 9.3.2 b - Interested parties and relevant issues AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 24
R Identifying internal issues.. at what level? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
Ronen E FDA News FDA issues guidance on bench testing in premarket submissions Other US Medical Device Regulations 0
P Why does the standard clause use the term Issues in place of Context - ISO 27001 4.1 IEC 27001 - Information Security Management Systems (ISMS) 3
Ashok sunder How to determine the internal and external issues in ISO 45001 standard? Occupational Health & Safety Management Standards 2
CCaantley Issues with Faro Quantum S and LLP General Measurement Device and Calibration Topics 0
M FDA News The FDA Issues Final Rule on Medical Device Classification Procedures Medical Device and FDA Regulations and Standards News 0
S Risk Approach doesn't address External Issues (Auditor's Comment) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 30
qualprod Closing Out Negative Issues in Context and Interested Parties ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
O Private label issues For EU - Customer does not have CE Mark CE Marking (Conformité Européene) / CB Scheme 7
O Examples of the external and internal issues and their risks and opportunities IATF 16949 - Automotive Quality Systems Standard 2
Y ISO 9001:2015 Cl. 4.1 Note 1 - External and Internal issues ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
bio_subbu Indian government issues guidance on Grouping Medical Devices in a Single Submission Other Medical Device Regulations World-Wide 1
qualprod External/internal issues removed as well? ISO 9001:2015 Cl. 4.1 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
bio_subbu India’s CDSCO Issues FAQ's on Medical Device Rule, 2017 Other Medical Device Regulations World-Wide 0
M Capturing Issues of Devices Past Lifetime Nonconformance and Corrective Action 3
A ISO 9001 Help - New Quality Manager - Upper Management Support Issues ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 23
A EMC Emission Issues - Communication between PC and Monitor IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
S Looking for an example of Issues Log ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
A One site of multi-site company closing - Quality transfer issues Quality Manager and Management Related Issues 7
Ronen E FDA issues draft guidance on form & content of UDI Other US Medical Device Regulations 0
Ronen E FDA issues draft guidance on additive manufacturing Other US Medical Device Regulations 1
L Packaging Issues Resulted CAR by customer Manufacturing and Related Processes 13
M What is the value of documenting in-process rework for easily-detectable issues? Quality Manager and Management Related Issues 4
bio_subbu USFDA issues draft Guidance on the Acceptance of Medical Device Clinical Data Other US Medical Device Regulations 1
M Issues with UDI additions to 21 CFR 820 requirements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
bio_subbu USFDA issues final guidance on "Reprocessing Medical Devices in Health Care Settings" Other US Medical Device Regulations 1
V What tool do you use for systemic issues? Problem Solving, Root Cause Fault and Failure Analysis 2
J CFDA issues Guiding Opinions on Enhancing the Construction of Food and Drug Inspectio China Medical Device Regulations 1
J Customer Complaint - PPAP - Issues not called out on the print APQP and PPAP 3
Marc FDA Issues Guidance On Cybersecurity of Medical Devices Other Medical Device and Orthopedic Related Topics 1
bio_subbu FDA issues Guidance on UDI - Frequently Asked Questions, Vol. 1 Other US Medical Device Regulations 1
bio_subbu FDA issues Small Entity Compliance Guidance for UDI Other US Medical Device Regulations 1
G VoIP PBX Development Issues Misc. Quality Assurance and Business Systems Related Topics 1
Ajit Basrur FDA issues Guidance Document - Benefits-Risks Factors to consider for 510(K) US Food and Drug Administration (FDA) 1
bio_subbu India's CDSCO issues a list of Medical Devices that require Registration Other Medical Device Regulations World-Wide 8
bio_subbu USFDA issues final guidance on Global Unique Device Identification Database (GUDID) Other US Medical Device Regulations 1
Ajit Basrur FDA issues Final Guidance on Mobile Medical Apps (Applications) US Food and Drug Administration (FDA) 2
C Buffer Media Validation Issues Design and Development of Products and Processes 3
W Customer Recommendation of Supplier - Qualification Issues Supplier Quality Assurance and other Supplier Issues 2
Pancho Quality Nightmare - Porsche 911 991 Issues Quality Manager and Management Related Issues 2

Similar threads

Top Bottom