Showing 1–50 of 55 results
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Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR: 2-day In-person Seminar
June 13-14,2019 - Philadelphia, PAView Details | Register -
21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar
June 13-14,2019 - Philadelphia, PAView Details | Register -
FDA’s New Import Program for 2019 – Strict Precision: 2-Day In-Person Seminar by Ex-FDA Official
June 18-19, 2019 - San Francisco, CAView Details | Register -
Designing and Sustaining New and Existing Product Stability Testing Program: 2-day In-person Seminar
June 20-21, 2019 - Atlanta, GAView Details | Register -
Managing Your FDA Inspection: Before, During and After: 2-Day In-Person Seminar by Ex-FDA Official
June 20-21, 2019 - San Francisco, CAView Details | Register -
Expense Reporting Best Practices: One and a Half Day In-Person Seminar
June 26-27, 2019 - New York, NYView Details | Register -
Accounts Payable Best Practices: One and a Half Day In-Person Seminar
June 27-28, 2019 - New York, NYView Details | Register -
Drug Master Files (DMF) – Translating FDA Guidances into Usable Documentation: One and a Half-day In-person Seminar
July 18-19, 2019 - San Diego, CAView Details | Register -
PV (Pharmacovigilance) Audit Strategy Planning – A Practical Approach to Design and Implementation: 2-Day In-Person Seminar
July 22-23, 2019 - San Francisco, CAView Details | Register -
SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations: 2-Day In-Person Seminar by Ex-FDA Official
July 25-26, 2019 - Philadelphia, PAView Details | Register -
REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance: 2-Day In-Person Seminar
August 1-2, 2019 - San Francisco, CAView Details | Register -
Quality Control Laboratory Compliance – cGMPs and GLPs: One and a Half-day In-person Seminar
August 15-16, 2019 - Philadelphia, PAView Details | Register -
FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials: 2-Day In-Person Seminar by Ex-FDA Official
August 15-16, 2019 - San Francisco, CAView Details | Register -
Biostatistics for the Non-Statistician: 2-Day In-Person Seminar
September 5-6, 2019 - Boston, MAView Details | Register -
Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar
September 26-27, 2019 - Boston, MAView Details | Register -
Change Control Best Practices – Avoiding Unintended Consequences of Changes: 2-Day In-Person Seminar
October 10-11, 2019 - Huntsville, ALView Details | Register -
FDA’s Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies: 2-day In-Person Seminar
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CAPA and its Strategy: Root Cause Analysis: 2-day In-person Seminar
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Building a Risk Based Internal Audit Plan: What Matters to the Organization: 2-Day In-person Seminar
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Beyond HIPAA: Developing Your Privacy and Information Security Programs in Healthcare Organizations: One and a Half Day In-person Seminar
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Smart Tax and Accounting Solutions for Small Business: 2-day In-person Seminar
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Biotech/Biosimilar Products: Current and Emerging Analytical CMC Expectations: 2-Day In-Person Seminar
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Enterprise Risk Management: 2-day In-person Seminar
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Statistical Analysis for Product Development: 2-day In-person Seminar
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Payroll Best Practices: 10 Areas You Must Handle Correctly to Ensure Compliance: One and a Half day In-Person Seminar
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Individual Tax Minimization Strategies for 2015: 2-day In-person Seminar
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TurboEIRs and their Use within Warning Letters to Illustrate the FDA and Health Canada CFRs: 2-Day In-Person Seminar
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California Laws Regulating Employment Screening and Safe Hiring: 2-Day In-Person Seminar
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Deviation Investigation Best Practices – Ensuring Correct Content and Conclusions: 2-Day In-Person Seminar
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Reducing Taxes and Managing Accounting for Efficient Business Investments: 2-day In-person Seminar
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Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices: 2-day In-person Seminar
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Global Food Supply Chain Risk and Blue Ocean Strategy Using Supply Chain Management: 2-day In-person Seminar
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Internal Control Best Practices for your Procure to Pay (P2P) Process: 2-Day In-Person Seminar
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Import Procedures and Documentation: 2-Day In-Person Seminar
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Quality Management, GMP and Regulations – Impact on Food, Seafood and Nutritional Supplements: 2-Day In-person Seminar
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Aseptic Processing Challenges: 2-Day In-Person Seminar
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Identity Theft Exposure and the Methods Utilized to Prevent and Detect the Transfer of Illegal Funds through Financial Institutions: 2-Day In-Person Seminar
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Fraud Evaluation Tools for the Internal Auditor: 2-Day In-Person Seminar
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Implementing a Basel III and COSO Compliant Operational Risk Management Program: 2-Day In-Person Seminar
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Internal Audits and Supplier Audits for Life Science Companies: 2-day In-Person Seminar
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Regulated Laboratory Inspections – Be Prepared, Be Validated and Avoid Observations: 2-Day In-Person Seminar
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Developing an Environmental Monitoring Strategy for a Non-Sterile and Aseptic Processing Area (Controlled/Classified Environment) — To Include HVAC and Utility Systems: 2- day In-person Seminar
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Forensic Accounting and Fraud Examination Exercises: 2-Day In-Person Seminar
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GMP Validation Workshop | Learn to create your own workshop and private sessions
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Best Strategies for Meeting US (IND through Post Marketing) Drug Safety Requirements Efficiently: 2-Day In-Person Seminar
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Building Your Business Internationally: How to successfully import and export: 2-day In-person Seminar
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Effective Service Level Agreements (SLAs) to Improve Business Services Level and Quality Using a Structured Risk Analysis Methodology: 2-Day In-person Seminar
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