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June 2007 Open Enrollment Calendar

Note: Courses mentioned represent the first day only.
Each course consists of two days of training.

JUNE2007
Sun.	Monday	Tuesday	Wednesday	Thursday	Friday	Sat.
					1	2
3	4 European Regulatory Affairs - AG237	5	6 Implementing Best Practices for Cleaning Validation - AD129	7 Auditing and Qualifying Suppliers and Vendors - AW217	8	9
10	11 CMC Requirements - AV921 Int'l GMPs: Complying w/Requirements in the U.S., EU and Japan - AC318 Implementing the CTD Format for NDA Submissions - AG236 Complying with FDA/ICH Requirements for Stability Testing - AL560	12 Monitoring and Reporting Adverse Drug Reactions - AV933 Auditing Clinical Trials for GCP Compliance - AH532	13 Auditing Clinical Trials for GCP Compliance - AH531	14 Mastering Biomedical Writing - AW219 Conducting Annual Product Reviews - AW238	15	16
17	18 PLC, SCADA and DCS: cGMP Qualification for Automated Process Control Systems - AE425 Clinical Statistics for Non-Statisticians - AH539 Complying with Computer and Software Validation Requirements - AE420 Complying With FDA Requirements For Labeling & Packaging - AW213 Aseptic Processing of Sterile Drug Products - AV927 Conducting Batch Record Reviews and Investigations - AW225	19 Implementing Key Requirements for Process Validation - AV931 Implementing Best Practices for Cleaning Validation - AD130 Electronic Records Compliance: A Risk-Based, Predicate Rule Approach - AE424 Good Clinical Practice (GCP) for Medical Devices - AM148	20 Navigating the Drug Development Lifecycle from Bench to Bedside - AH534 Introduction to Good Manufacturing Practices (GMPs) - AC314	21 Achieving and Maintaining Laboratory cGMP Compliance - AL564 Project Management in Drug Development: Phase I and Phase II - AP166	22	23
24	25 Mastering Your Performance as a QA Professional - AW232 & AW233 Project Management in Drug Development: Discovery and Preclinical - AP164 Writing Standard Operating Procedures (SOPs) - AW237 Int'l GMPs: Complying w/Requirements in the U.S., EU and Japan - AC319 Improving the Performance of Your Lyophilization System - AG234 Complying with Computer and Software Validation Requirements - AE421 CMC for Biopharmaceuticals - AV932 Complying With FDA Requirements For Labeling & Packaging - AW214	26 RFID and Secure Supply Chain Systems - AL568 Implementing Clinical Trial Performance Metrics - AH540 Project Management in Drug Development: Phase III and Commercialization - AP162	27	28	29	30

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