Conferences and seminars
Eventos: Conferências, seminários, workshops ...Conferences and seminars complianceonline (Total 109, Página 4 / 6)
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Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Supplier and Contract Manufacturer Management for Medical Device Manufacturers
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Analytical Instrument Qualification and System Validation
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus)
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Sustainable Compliance for Out of Specifications (OOS) Results, Deviations, and Corrective and Preventive Actions (CAPA)
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Building a Vendor Qualification Program for FDA Regulated Industries
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
SOP Writing, Training and Compliance in the Pharmaceutical Industry
SanJose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Data Integrity: FDA, WHO and EMA's Requirements
SanJose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
San Jose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
SanJose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Analytical Instrument Qualification and System Validation
SanJose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Data Integrity: FDA/EMA Requirements and Implementation
SanJose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
Radiation Sterilization of Medical Products - Beyond the Basics
SanJose, Estados Unidos
Saúde e Medicina Regulation in Medicine and Pharmacology
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