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Upcoming In-person and Virtual Seminars by Ex-FDA and other regulatory experts.
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Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
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* For one Registration $1899

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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* For one Registration $1899

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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* For one Registration $699

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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* For one Registration $1999

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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* For one Registration $1099

 

 

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