Training

IPA Consulting Services offers many opportunities to achieve technical and operational excellence in the pharmaceutical, biotechnology, Medical Device and Nutraceutical industries. Our team of expert consultants consists of industry professionals, academia and former government inspectors.

Covering over five distinct areas of topics; compliance, regulatory, validation, Laboratory, and manufacturing with delivery in every corner of the United States, Canada, Europe and Asia, we guarantee you'll find the answers to your most pressing questions. We are dedicated to identifying your training objectives and converting your training investment into meeting your corporate compliance goals.

Here at IPA Consulting Services, we partner with our clients to provide effective customized training in short course formats together with carefully orchestrated workshops that fits their educational needs and budget.

We offer a broad range of training workshops

Compliance

• GMP for Pharmaceuticals
  
• GMP Issues for Biopharmaceuticals and Vaccines
  
• GMP for Nutraceuticals
  
• GMP for Medical Devices
  
• Technical Writing
  
• Pre-Approval Inspection
  
• Implementation of Change Control Program
  
• Investigation of Out-of-Specification Results
  
• Root Cause Analysis for CAPA
  
• Effective Quality Assurance Auditing
  
• SOP, Reports, Protocols and Quality Manual Preparation
  
• Third Party Audit & Supplier Qualification
  
• Complaints and Recalls
  
• Implementation of Risk Management
  
• Annual Product Review

Manufacturing

• Optimizing Drug Formulation
  
• Tablet Formulation and Technology
  
• Capsulation
  
• Aseptic Processing
  
• Pharmaceutical Packaging

Validation

• Cleaning Validation
  
• Process Validation
  
• Cleanroom
  
• Validation of Computer Systems
  
• Process Validation
  
• Facility and Utilities Qualification
  
• Cold Chain
  
• Biological and Vaccine Manufacturing Process Validation
  
• Environmental Monitoring
  
• Biostatistics for Non Statisticians
  
• Water Systems Validation

Laboratory

• HPLC Method Validation
  
• Method Development
  
• Dissolution Testing
  
• Technology Transfer
  
• Microbiological Assay
  
• Stability Program

European Regulatory Affairs

• European Regulatory Affairs
  
• Canadian Regulatory Affairs
  
• US Regulatory Affairs
  
• Adverse Drug Reporting
  
• ICH Guidelines
  
• Project Management for Clinical Trials
  
• Batch Record Review and Approval