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
Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
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Latin America: Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs)
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Data Integrity: FDA, WHO and EMA's Requirements
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FDA's Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering
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Statistics for Quality Control
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Integrating Design Controls and the Product Development Process for Effective and Compliant Medical Device Development
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The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities
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AML/BSA Boot Camp
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In Depth EU Medical Device Regulation (MDR) 2017/745 Training
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Statistical Elements of Post Market Clinical Follow-up (PMCF)
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A Comprehensive View of FDA Regulations for Medical Devices
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How to Implement MDSAP-Requirements into Your ISO 13485 Quality Management System?
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Medical Device Software Validation Training - IEC 62304
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Basel III, IV and Beyond - Effective Risk Data Management and Reporting
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Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
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Auditing and Compliance - International Trade Finance
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PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation
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Technical Writing for Pharma, Biotech and Medical Devices
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A risk based approach to GxP Compliant Laboratory Computerized Systems
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The Drug Development Process from Concept to Market
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