"Todays Active Topics" a suggestion.

Geoff Cotton

Quite Involved in Discussions
#1
Mark,

Any chance of extending the "Todays Active Topics" link to cover more than 24 hours?

In the UK we are missing posts to the forum due to the different time zones.

Geoff
 
Elsmar Forum Sponsor

Marc

Hunkered Down for the Duration
Staff member
Admin
#2
I'll take a look at the perl scripts in the next week or 2 - but don't get your hopes up. The perl is pretty weird. In fact, I stopped upgrading the software as every update was more buggy than the last. The ultimatebb folks kept adding features but introducing more bugs without fixing all the old bugs.
 
Thread starter Similar threads Forum Replies Date
Marc Todays Topic: Learn Spanish! Coffee Break and Water Cooler Discussions 5
T Loaded spring device - Active medical device? EU Medical Device Regulations 1
P MDR Rule 10 interpretation - Active Device EU Medical Device Regulations 3
N Question on creepage/clearance requirements for HF Active Accessories for 2nd edition 60601-1 IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
M Active Surface Disinfectant Claims - FDA vs EPA and Hands vs Objects Other Medical Device and Orthopedic Related Topics 0
S Acrylic in Class II b Active Medical Device IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
P Non-Active Suppliers on CE Certificate EU Medical Device Regulations 2
Y Informational Change control process - Major vs Minor change - Active class III medical devices ISO 13485:2016 - Medical Device Quality Management Systems 12
M Medical Device News TGA Consultation: Potential reclassification of active medical devices for diagnosis and patient therapy Medical Device and FDA Regulations and Standards News 0
D Used active medical devices 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
chris1price Are these Active Medical Devices? EU Medical Device Regulations 17
J Label on Miniature Active Class I Medical Device EU Medical Device Regulations 0
M Incomplete Unannounced Audit - No Active Production at the time ISO 13485:2016 - Medical Device Quality Management Systems 11
M IEC 60601-1 and Active Current Protection Requirements IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
S 100% Final Inspection Requirements of Active Medical Devices (MDD or IEC Standards?) EU Medical Device Regulations 4
P Medical Device changes - Active implants EU Medical Device Regulations 2
A Active Implantable Medical Devices - Legal Traceability Requirements ISO 13485:2016 - Medical Device Quality Management Systems 7
M Active X and latest update from Microsoft - Dec 2014 After Work and Weekend Discussion Topics 4
R Cable used in Active Implantable Medical Device Other Medical Device and Orthopedic Related Topics 4
F ASQ chapter 1423 is now active in Lafayette ASQ - American Society for Quality 2
J Risks Analysis of an Active Implantable Muscle Stimulator ISO 14971 - Medical Device Risk Management 8
C Application of IEC 62366 - Usability of Non-Active Medical Devices IEC 62366 - Medical Device Usability Engineering 15
D Device that makes another Device (Active Implant Medical Device) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
G 510K for Active Medical Device - IEC 60601-1 or UL 60601-1 Compliance Other US Medical Device Regulations 3
A Does my Product (Active Machine Support Frame) require CE Marking CE Marking (Conformité Européene) / CB Scheme 4
P How to get FDA Approval of an API (Active Pharmaceutical Ingredients) Plant in India US Food and Drug Administration (FDA) 3
P FDA Approved API (Active Pharmaceutical Listing) Bioequivalence Study Lab for India Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
W Pro-active Quality Culture Improvements - Suggestions, Tools and Techniques Quality Tools, Improvement and Analysis 3
M Internal Auditing of Area with Active Change Control Internal Auditing 14
W ISO 9001 Certified - Active Six Sigma - What Next? Quality Manager and Management Related Issues 25
A Software Validation Requirements for Class I Active Medical Device EU Medical Device Regulations 4
W APM (Active Patient Monitoring) - FDA vs. EU Requirements and Classifications ISO 13485:2016 - Medical Device Quality Management Systems 2
R Definition Active Medical Device - Clarification of definition Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 6
H Active Parts with No FAI - How far back do you go? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
somashekar Making permanent savings through Active Energy Efficiency Sustainability, Green Initiatives and Ecology 7
N RFID on a Medical Disposable Kit - Active Medical Device? IEC 60601 - Medical Electrical Equipment Safety Standards Series 14
T Validation of water system in API (Active Pharmaceutical Ingredients) unit Qualification and Validation (including 21 CFR Part 11) 5
R Process Validation Issues - Active Pharmaceutical Ingredients Qualification and Validation (including 21 CFR Part 11) 2
R Facility qualification - API (Active Pharmaceutical Ingredient) industry Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 11
R Application of MSA in Pharmaceutical (Active Pharmaceutical Ingredient) industries Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
R Quality Management System not active for 6 months. Registration let it Lapse or Fail? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
G New intended use - Validation of a class IIb implantable (non-active) ISO 13485:2016 - Medical Device Quality Management Systems 5
T How should I define a process-The use of the Active Voice Process Maps, Process Mapping and Turtle Diagrams 14
I Active Medical Devices - An example of an Active Medical Device and Definition EU Medical Device Regulations 4
J Requirements for Implantation Records/Cards - Class III, Implantable (not active) ISO 13485:2016 - Medical Device Quality Management Systems 1
H Links in Posts - Post Counts and Active Links in Posts Elsmar Cove Forum ToS and Forum Policies 8
O NDCs and Cosmetics that contain a "Drug Product Active Ingredient" US Food and Drug Administration (FDA) 3
J What Can You Do with Active Server Pages? Quality Tools, Improvement and Analysis 0
E Customer Satisfaction - Active and Passive - Simple explanation of the difference ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
A Multiple active revsions Document Control Systems, Procedures, Forms and Templates 5

Similar threads

Top Bottom