22 courses listed below. |
|
|
Title
|
Date
|
Location
|
Hours
|
Pharmaceutical Engineering Courses |
 Practical Pharmaceutical Process Scale-Up K942 |
Nov 16-17, 2009 |
Las Vegas, NV |
12 |
| Statistical Design of Experiments (DoE) for Pharmaceutical Process R&D and Manufacturing: A Practical Approach K964 |
Mar 8-10, 2010 |
Las Vegas, NV |
18 |
| Tablet and Capsule Manufacturing: Introduction and Update for Competitive Organizations L272 |
Mar 15-17, 2010 |
Las Vegas, NV |
18 |
| Practical Approaches to Quality by Design (QbD) for Pharmaceutical Process Development and Manufacturing L037 |
Apr 12-14, 2010 |
Las Vegas, NV |
18 |
| Auditing Domestic and International Suppliers to the Pharmaceutical Industry L273 |
Apr 19-20, 2010 |
Las Vegas, NV |
12 |
| Practical Pharmaceutical Process Scale-Up K963 |
Apr 26-27, 2010 |
Las Vegas, NV |
12 |
| Advanced Practices in Pharmaceutical Tablet and Capsule Technology L139 |
May 3-5, 2010 |
Las Vegas, NV |
12 |
| Test Method Validation in Pharmaceutical and Biopharmaceutical Development and Production G334 |
schedule with EPD |
at your site |
|
| Pharmaceutical Water Systems G336 |
schedule with EPD |
at your site |
|
| Evaluating Raw Materials for the Development of Biopharmaceutical Products H880 |
schedule with EPD |
at your site |
|
| Auditing Suppliers to the Pharmaceutical Industry J125 |
schedule with EPD |
at your site |
|
| Developing and Implementing Effective Pharmaceutical Stability Programs J126 |
schedule with EPD |
at your site |
|
| Best Practices in Biopharmaceutical Raw Materials Testing and Vendor Qualification J127 |
schedule with EPD |
at your site |
|
| Cleaning Validation Practices for Pharmaceutical and Biopharmaceutical Production J128 |
schedule with EPD |
at your site |
|
| Pharmaceutical and Device Project Management J130 |
schedule with EPD |
at your site |
|
| Writing and Managing Pharmaceutical SOPs in Compliance with cGMP J131 |
schedule with EPD |
at your site |
|
| Pharmaceutical Laboratory Controls for FDA Compliance: A Systematic Priority-Setting Approach J132 |
schedule with EPD |
at your site |
|
| GMPs and Application of Quality Systems to Dietary Supplements: Strategies to Achieve Compliance K888 |
schedule with EPD |
at your site |
|
| Statistical Design of Experiments (DoE) for Pharmaceutical Process R&D and Manufacturing: A Practical Approach K889 |
schedule with EPD |
at your site |
|
| Active Pharmaceutical Ingredient (API) Crystallization: A Practical Approach to Process Research, Development, and Scale-Up K890 |
schedule with EPD |
at your site |
|
| Practical Pharmaceutical Process Scale-Up K892 |
schedule with EPD |
at your site |
|
| Cleaning Validation Practices for Pharmaceutical and Biopharmaceutical Production J996 |
TBA |
|
12 |
