In-Company Training Program 2011
| Location | Course | Language | Duration | Date | Price | |
|---|---|---|---|---|---|---|
At your company |
on request! | 1 day | - |  |
||
At your company |
2-Comprehencive study of ISO 13485 and a relation with ISO 14971 |
on request | 2 days | - | contact us |
|
At your company |
on request | 2 days | - | contact us |
|
|
At your company |
4-Internal auditor FDA 21 CFR 820 Quality Systems Regulations- A Practical Guide | English | 2 days | - | contact us |
|
| At your company | 5-Internal auditor ISO 13485 & 21 CFR 820 Quality System Regulations-A Practical Guide | English | 2 days | - | contact us |
|
| At your company | 6-Supplier auditing - Intrument to control your suppliers and subcontractors | English | 1 day | - | contact us |
|
| At your company | 7-Risk Management for Medical Devices ISO 14971 using FMEA | English | 1 day | - | contact us |
|
| At your company | 8-Introduction to the European Medical Device Directives - A better understanding | English | 1 day | - | |
|
| At your company | 9-Medical Device Regulations in the European Union: CE marking in detail | English | 2 days | - | contact us |
|
| At your company | 10-Medical Device Classification & Conformity Assessment Routes with a focus on Europe, Australia, USA and Canada | English | 1 day | - | contact us |
|
| At your company | 11-Post Market Surveillance & Vigilance with a focus on Europe, USA, Canada, Australia and Japan | English | 1 day | - | contact us |
|
| At your company | 12-How to construct a Technical File for Worldwide use - STED model of the GHTF | English | 1 day | - | contact us |
|
| At your company | 13-Clinical Evaluation of Medical Devices including Post Market Clinical Follow-up, using ISO 14155 & MEDDEV 2.7 | English | 1 day | - | contact us |
|
| At your company | 14-Introduction to Biocompatibility ISO 10993 series - a better understanding | English | 1 day | - | |
|
| At your company | 15-Medical Devices Process Validation - IQ/OQ/PQ | English | 1 day | - | |
|
| At your company | 16-Introduction to FDA 21 CFR 820 Quality System Regulations | English | 1 day | - | contact us |
|
| At your company | 17-Introduction to FDA 21 CFR 11: Electronic Records; Electronic Signatures | English | 1 day | - | contact us |
|
| At your company | 18-FDA's 510(k) & PMA submissions - explained in detail | English | 2 days | - | contact us |
|
| At your company | 19-FDA's pre-IDE process - explained in detail | English | 1 day | - | contact us |
|
At your company |
20-Introduction to SOR/98-282 Canadian Medical Devices Regulations - a better understanding | English | 1 day | - | |
|
| At your company | 21-Design Control for a Medical Device Manufacturer - A comprehensive model | English | 2 days | - | contact us |
|
At your company |
22-Introduction to Practical Project Management | English | 1 day | - | contact us |
|
| At your company | 23-Introduction to sterilization and (microbiological) validation process - An overview | English/Dutch | 1 day | contact us |
|
|
For the complete training program: 