SEMINARS
Upcoming In-person and Virtual Seminars by Ex-FDA and other regulatory experts.
Get Trained on - FDA Audits and Inspections, FDA’s GMP Expectations, Clinical Trials, Vendor Selection, FDA’s New Import Program, FDA Recalls, CAPA and more
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
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Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval
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How to Write Error Free Procedures and Instructions
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Supplier and Contractor Qualification and Control for Life Science Industry
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CGMP Quality Principles for the FDA Regulated Industries
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The New OSHA Recordkeeping Rule & Surviving An OSHA Audit
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REACH and RoHS Compliance: Gain a Deeper Understanding
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Incorporating Risk Management in your HR policy
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How to Create Excel Dashboards Using Pivot Tables
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FDA Requirements for Food Defense Planning and Implementation
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Effective Design, Validation and Routine Maintenance of Pharmaceutical Gases
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Data Integrity: FDA/EMA Requirements and Implementation
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GMP Compliance for Quality Control and Contract Laboratories
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Data Integrity: FDA/EU Requirements and Implementation
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Understanding the FDA's Regulation of HCT/Ps and Successful Product Development Strategies
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Computer System Validation - Reduce Costs and Avoid 483s
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Effective Design, Validation and Routine Maintenance of Pharmaceutical Water
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Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
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Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
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GMP Compliance for Quality Control and Contract Laboratories
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