Workshops
Please choose one of the following workshops below to get more information about each workshop
| EVENTS |
DATE |
| Batch Record review and Investigation * |
February 15, 2012 |
| Supplier Quality Agreement, Supplier Quality Audit and Qualification * |
February 15, 2012 |
| Medical Device Quality & Regulatory Requirements for Importer/Distributor and Manufacturers – Canadian Market * |
February 28, 2012 |
| Conducting Effective Annual Product Review * |
March 26-27, 2012 |
| Conducting Effective Auditing of GMP Documentations * |
March 28-29, 2012 |
| Development, Validation, Verification and Transfer of Analytical Methods * |
March 28-29, 2012 |
| Conducting Effective Investigations of Atypical and Out of Specification Laboratory Results * |
April 19, 2012 |
| Practical Pharmaceutical Manufacturing * |
April 19-20, 2012 |
| Quality Risk Managment - Risk Analysis, Mitigation and Management * |
May 10-11, 2012 |
| Best Practices - Cleaning Validation * |
May 10-11, 2012 |
| Environmental Control and Monitoring * |
June 14-15, 2012 |
| Standard Operating Procedure * |
June 14-15, 2012 |
| Laboratory Inspections * |
Sep 19, 2012 |
| CMC for Pharma and Biopharma * |
Sep 19, 2012 |
| Change Control and Deviations * |
Oct 17, 2012 |
| Residual Solvents * |
Oct 17, 2012 |
| Medical Devices * |
Nov 15, 2012 |
| Project Management for Pharma and Biopharm * |
Nov 15-16, 2012 |
| CAPA * |
Dec 11, 2012 |
* AAPS Facilities, In-house Training
