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Pharmaceutical Training Courses

Pharmaceutical Training Courses ()

cGMP guidelines/trends in HVAC Qualification/Validation for Pharmaceutical Sterile and non-Sterile Facilities/Projects
Risk-Based Approach for Commissioning, Qualification & Validation in Pharmaceutical Industries/project (ASTM 2500 and ISPE Baseline Guide for Commissioning and Qualification 2019)-
Introduction for Water Purification, Storage and Distribution System in Pharmaceutical/ healthcare industries (Purified Water System)
Streamlined Approach for Moist Heat Sterilization (Autoclave) in Pharmaceutical and Healthcare Industries
Regulatory Streamline Approach for Design, Validation & Qualification of Pharmaceutical Manufacturing Facilities & Equipment Oral Solid Dosage Forms (21 CFR Part 211)
Environmental Monitoring for Pharmaceutical Facilities (ISO 14644 Compliance)
Building Validation and Qualification Master Plan (VMP/QMP)
Good Maintenance Practices in pharmaceutical industries
Streamline approach for Warehouse and Storage spaces Mapping ,Qualification and Calibration Methodologies/Requirements
Understanding the Role of Applied Statistics in Pharmaceutical Process Monitoring and Control
Pharmaceutical Quality by Design
Training Program for Pharmaceutical Manufacturing Operators and Supervisors
Good Engineering Practices in Pharmaceutical Industries
The Calibration in the Pharmaceutical industry; Fundamental, Concept and Risk based calibration approach
Business Success in the Pharmaceutical industry
Maintenance, Reliability and Engineering Excellence
Operations Research- Practical Quantitative Methods
Streamlined approach for Operations Management and Operational Excellence in the Pharmaceutical industry
Compressed Air system Qualification and testing
Equipment/Machine Software Validation According to 21 CFR Part 11 ,EU Annex 11 & GAMP 5 (Embedded and Computerized Software for pharmaceutical Equipment)
Serialization in the Pharmaceutical Industry (Global Track & Trace)
Quality Risk Management (QRM) in Pharmaceutical Industry
Environmental monitoring and handling temperature excursions
Streamlined Approach for Good Procurement Management in Pharmaceutical Industry
Common Technical Documents (CTD) Dossier: Requirements, Preparation, and Submission ((US, Europe and Jordan and KSA))
Drug Life Cycle
Regulatory Requirement for Medical Devices / Europe and its application
Pharmacovigilance and Vigilance
Equipment Criticality and Risk Based Requalification
Building effective Qualification protocols for Non-Sterile Pharmaceuticals Manufacturing Equipment
The Validation Manger & Management in the Pharmaceutical industry
Cost Saving and Lean Manufacturing for Pharmaceutical Facilities
Streamlined approach to Pharmaceutical packaging designs and operations (Scientific writing skills)
Risk Based Approach for Pharmaceutical Process Validation & Relevant Documentations
Risk Based Approach for Pharmaceutical Solid Dosage Forms Development
fundamentals of technology transfer and Relevant R&D activities
Fundamentals and streamlined approach for Pharmaceutical Microbiology
Fundamental and Cleaning Validation Best Practices
Handling of Deviation management and CAPA
Quality Audits (internal and external)
Handling Out of Specifications (OOS)
Good Laboratory Practices in Pharmaceutical Industry (GLP)
Good Storage and Distribution Practices (GSDP)

Cours de formation pharmaceutique

Nos cours de formation pharmaceutique sont classés comme:

Industrie pharmaceutique

Cours de formation en ingénierie et validation
Cours de formation de qualité
Cours de formation aux opérations
Cours de formation en laboratoire
Cours de formation en recherche et développement
Cours de formation

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