مؤتمرات وملتقيات علمية و ندوات
الأحداث : المؤتمرات والندوات وورش العمل ...مؤتمرات وملتقيات علمية و ندوات complianceonline (مجموع 109, صفحة 4 / 6)
ترتيب حسب: تاريخ البداية • أحدث الإضافات • الأكثر شعبية
Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Supplier and Contract Manufacturer Management for Medical Device Manufacturers
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Analytical Instrument Qualification and System Validation
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus)
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Sustainable Compliance for Out of Specifications (OOS) Results, Deviations, and Corrective and Preventive Actions (CAPA)
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Building a Vendor Qualification Program for FDA Regulated Industries
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
SOP Writing, Training and Compliance in the Pharmaceutical Industry
SanJose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Data Integrity: FDA, WHO and EMA's Requirements
SanJose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
San Jose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
SanJose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Analytical Instrument Qualification and System Validation
SanJose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Data Integrity: FDA/EMA Requirements and Implementation
SanJose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
Radiation Sterilization of Medical Products - Beyond the Basics
SanJose, الولايات المتحدة
الصحة والطب Regulation in Medicine and Pharmacology
العلامات
Military;
