Importing Address Books (Thunderbird and Outlook Express) into Windows Live Mail

Stijloor

Stijloor

Staff member
Super Moderator
#1
#1
Friends,

I need to import two address books (from Thunderbird and Outlook Express) into Windows Live Mail (my new Windows 7 laptop). Any ideas, suggestions on how to do this? All 3 machines are on the same office server.

Thank you so much for your help. :agree1:

Stijloor.
 
GAGEpack - Gage & Calibration Management
Elsmar Forum Sponsor
Stijloor

Stijloor

Staff member
Super Moderator
#3
#3
Stijloor said:
Friends,

I need to import two address books (from Thunderbird and Outlook Express) into Windows Live Mail (my new Windows 7 laptop). Any ideas, suggestions on how to do this? All 3 machines are on the same office server.

Thank you so much for your help. :agree1:

Stijloor.
Click to expand...
One last try...:(
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
D Importing a general wellness low risk product Other US Medical Device Regulations 3
I Importing prototype without CE (dos and don'ts ) EU Medical Device Regulations 11
S Importing Medical devices class I in EU Other Medical Device and Orthopedic Related Topics 5
O Importing a Medical Device into the US from abroad 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 13
M Importing a Registered Class II Device, the Applying Our Label - Need New 510(k)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
F Mexico Medical Device Importing and Servicing Other Medical Device Regulations World-Wide 2
ScottK Importing medical device for use in fit testing of packaging Other US Medical Device Regulations 3
M Importing medical devices to EU, Germany EU Medical Device Regulations 6
M Importing a Demo Medical Device into the US US Food and Drug Administration (FDA) 3
J Requirements for Importing Research Use Only Medical Devices into Japan Japan Medical Device Regulations 1
J Importing a Finished Medical Device from China (tooth whitener w/ peroxide) China Medical Device Regulations 2
O Importing Data via Script - Assign Column as Text (Minitab) Using Minitab Software 3
W What Information is provided when Importing Products into USA US Food and Drug Administration (FDA) 1
T Importing Non-Electromedical Device (PACS Software) into South Africa Other Medical Device Regulations World-Wide 2
S Importing a DC motor to UK that is less than 50VDC CE Marking (Conformité Européene) / CB Scheme 11
P Requirements for Importing Hydrocolloid Bandages into the US from China Other US Medical Device Regulations 2
Q FDA Registration and Importing Medical Device Components 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
M South Korea Importing Rules for Privately Labeled Medical Devices Advice wanted Other Medical Device Regulations World-Wide 5
N Importing Diagnostic kit from US, UK Other Medical Device Regulations World-Wide 5
B Class I Medical Device Importing for OEM Requirements EU Medical Device Regulations 3
A Importing Sample Medical Devices into South Korea ISO 13485:2016 - Medical Device Quality Management Systems 2
M Importing Material before the 510(k) is Approved 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
M Importing CE marked Syringes Into the US Other US Medical Device Regulations 2
I Importing Medical Devices into the USA from Germany (Drop Shipments) US Food and Drug Administration (FDA) 2
D Importing Class II Male Latex Condoms From China to US Other US Medical Device Regulations 2
L Importing exempt Class I device from non-registered manufacturer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
R Importing Breathalyzers into the USA 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
G Importing Medical Device Software to India - Diagnostic Imaging Application Other Medical Device Regulations World-Wide 8
L Importing CSV (comma separated values) / Excel process steps into Visio diagram Excel .xls Spreadsheet Templates and Tools 2
S Exporting then re-Importing 510(k) device 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
S Regulations for importing an IVD diagnostic test in India Other Medical Device Regulations World-Wide 16
bio_subbu CDSCO?s checklist on importing non-critical IVD products in India Other Medical Device Regulations World-Wide 1
amjadrana Importing Medical Devices with Computers as part of the device in Turkey Other ISO and International Standards and European Regulations 1
D Medical Device Regulations - Importing to Singapore - Orthodontic brackets Other Medical Device Regulations World-Wide 5
D How to obtain NOC from DCGI (Drug Controller General of India) for importing drugs Manufacturing and Related Processes 6
G Portocal II - Importing procedures Calibration and Metrology Software and Hardware 2
H Regulation in Australia - Importing medical device (class IIa as per MDD 93/42/EEC) ISO 13485:2016 - Medical Device Quality Management Systems 3
Ed Panek How to address a QMS Entry Error ISO 13485:2016 - Medical Device Quality Management Systems 8
P Update on NBOG 2014-3 to address MDR/IVDR, or any plan to do that? EU Medical Device Regulations 0
M Address change for a company with CE/ISO13485 EU Medical Device Regulations 2
J FDA notification of address change US Food and Drug Administration (FDA) 2
R Where does IATF 16949 address Process mapping? IATF 16949 - Automotive Quality Systems Standard 3
N Address of Legal Manufacturing Site in ISO 13485 certificates? ISO 13485:2016 - Medical Device Quality Management Systems 1
Ajit Basrur Physical Address on Product Labels (EU MDR perspective) EU Medical Device Regulations 2
A How to address Environmental & OHS Opportunities? ISO 14001:2015 Specific Discussions 6
Q Legal Manufacturing Address Change – multiple registrations at same address 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
K Changing the Address in 510(K) Approved Product 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
E Received a Major finding during IATF Surveillance audit for loss of BIQS Level 3 (more than 6 SPPS in 6 months)...how should we address SYSTEMIC CA? IATF 16949 - Automotive Quality Systems Standard 11
M Manufacturer address on the label Other US Medical Device Regulations 18
M GDPR - Is anonymizing sufficient to address right to erasure? Medical Information Technology, Medical Software and Health Informatics 3

Similar threads

Top Bottom