1728333.1000|^|000037|^||^||^||^|20-1001000|^|no|^|
2451027.2235|^|000000|^|Retention time for Quality records|^|14|^|Monica Lewis|^|199808012235|^|no|^|
2451029.0828|^|000002|^|Problem with Forum|^|0|^|Marc Smith|^|199808030828|^|no|^|
2451029.0928|^|000003|^|Design Control (Monica Lewis)|^|0|^|Marc Smith|^|199808030928|^|no|^|
2451030.2246|^|000005|^|Quality Records - Storage|^|2|^|Marc Smith|^|199808042246|^|no|^|
2451031.1915|^|000007|^|EN46001 & ISO13485|^|2|^|Roger Eastin|^|199808051915|^|no|^|
2451035.2208|^|000008|^|Auditing Guidelines|^|3|^|Marc Smith|^|199808092208|^|no|^|
2451043.0509|^|000004|^|The Don Winton Memorial FDA Stuff Archive|^|3|^|Marc Smith|^|199808170509|^|no|^|
2451071.2159|^|000009|^|War Stories|^|0|^|Don Winton|^|199809142159|^|no|^|
2451100.2026|^|000010|^|CE Mark Myths|^|2|^|Marc Smith|^|199810132026|^|no|^|
2451130.1329|^|000011|^|Value of ISO9000 for a clinic|^|2|^|Roger Eastin|^|199811121329|^|no|^|
2451131.1007|^|000012|^|definition|^|3|^|Monica Lewis|^|199811131007|^|no|^|
2451192.1056|^|000013|^|Design input|^|1|^|Monica Lewis|^|199901131056|^|no|^|
2451212.0823|^|000014|^|Must everything be signed and dated?|^|3|^|Monica Lewis|^|199902020823|^|no|^|
2451250.1656|^|000015|^|Design validation|^|5|^|Monica Lewis|^|199903121656|^|no|^|
2451265.0037|^|000016|^|Classification rules for Canada|^|8|^|Mike|^|199903270037|^|no|^|
2451325.1132|^|000019|^|Design History File|^|1|^|Mark Smith|^|199905261132|^|no|^|
2451347.1057|^|000020|^|Graphical Symbols|^|1|^|SwidenS|^|199906171057|^|no|^|
2451479.1005|^|000021|^|Auditing Development|^|5|^|Mark Smith|^|199910271005|^|no|^|26
2451504.0647|^|000022|^|EN46001 and EN46002|^|4|^|Marc Smith|^|199911210647|^|no|^|24
2451509.1728|^|000023|^|Purchase |^|3|^|Monica Lewis|^|199911261728|^|no|^|19
2451534.0953|^|000025|^|Design Control Necessary|^|2|^|Nilar Divad|^|199912210953|^|no|^|1
2451546.2228|^|000024|^|ISO13485 ISO13488 vs EN46000 Series|^|1|^|Marc Smith|^|200001022228|^|no|^|22
2451571.0635|^|000018|^|technical reports|^|13|^|barb butrym|^|200001270635|^|no|^|
2451578.1523|^|000026|^|Internal Audit for FDA|^|0|^|Marc Smith|^|200002031523|^|no|^|5
2451599.0854|^|000027|^|Process monitoring|^|1|^|G.Hester|^|200002240854|^|no|^|3
2451648.0910|^|000028|^|Verification Activities|^|1|^|Mark Smith|^|200004130910|^|no|^|15
2451655.2012|^|000017|^|Medical Device Industry Links|^|4|^|Marc Smith|^|200004202012|^|no|^|
2451661.1521|^|000029|^|Continuous Certification|^|3|^|ISO GUY|^|200004261521|^|no|^|12
2451662.1336|^|000030|^|FDA documentation|^|0|^|A.Tremer|^|200004271336|^|no|^|26
2451666.1310|^|000031|^|ISO 13485:1996|^|2|^|Marc Smith|^|200005011310|^|no|^|5
2451676.2208|^|000033|^|FDA  and Documentation|^|0|^|Marc Smith|^|200005112208|^|no|^|23
2451720.1148|^|000034|^|New Medical Device Forum|^|0|^|Marc Smith|^|200006241148|^|no|^|14
2451736.1702|^|000035|^|Special Processes|^|0|^|Wallybaloo|^|200007101702|^|no|^|15
2451754.1042|^|000036|^|Passivation Validation|^|1|^|Tim Mosher|^|200007281042|^|no|^|18
2451815.0926|^|000032|^|EN46000|^|2|^|ALM|^|200009270926|^|no|^|5
2451947.1504|^|000038|^|FDA|^|2|^|Lee Clermomnt|^|200102061504|^|no|^|1
2451962.1345|^|000039|^|QSRs and ISO 9001 -2000|^|1|^|Greenraisin|^|200102211345|^|no|^|1
2451967.1107|^|000040|^|Seeking CQE for Med Devices - NJ|^|0|^|P2000MC|^|200102261107|^|no|^|1
2451969.2102|^|000041|^|Need Director of Quality in Orlando|^|0|^|LauraElliott|^|200102282102|^|no|^|1
2452032.0943|^|000043|^|QSR Purchasing Controls governing evaluation and use of consultants|^|1|^|Mikea|^|200105020943|^|no|^|5
2452038.1005|^|000042|^|Electronic Records and Signatures|^|1|^|Marc Smith|^|200105081005|^|no|^|28
2452051.0852|^|000044|^|ISO 13485|^|0|^|ISO GUY|^|200105210852|^|no|^|5