PTI Global provides customised onsite training for the pharmaceutical industry.
Benefits of onsite training:
Please click here for more information on how PTI can help you achieve your training goals.
PTI Europe courses are now recognised by the CPD Certification Service. For further information or to devise your own CPD record or development plan, please click on the links below.
CPD Personal Development Plan
Need Accommodation? PTI has arranged a special room rate with Hotel Map at a number of hotels.
Understanding and Preparing the Quality and Pharmaceutical Module of the Global CTD Dossier
Mastering Regulatory and Development Strategies for Generics
Risk-Based Monitoring & Targeted SDV
Regulatory Affairs for Biopesticides
Analysing and Validating Biological Assays
EU and US Requirements for Pharmaceutical Labelling & Package Leaflets
Effectively Managing Vendor Oversight
Introduction to Regulatory Affairs for Medical Devices
Advanced European Regulatory Affairs
Clinical Research Project Management
Introduction to Toxicology for the Non-specialist
Advanced Regulatory Affairs for Medical Devices
Budget Management for Clinical Trials
Registering Agrochemicals in the EU
An Introduction to Pharmacovigilance
Introduction to Pharmacokinetics for the Non-Specialist
Introduction to European Regulatory Affairs
Gaining Marketing Authorisations in CIS
EU Biosimilar Registration and Marketing Requirements
Antibody Display, Selection and Engineering
Best Practice for Clinical Monitors and CRAs
Regulatory Affairs Strategies
Signal Detection Strategies
Regulatory Affairs for Veterinary Medicines
CMC Analytical, Comparability and Stability Studies for Biotechnology Products
Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
Intermediate Pharmacovigilance and Adverse Event Reporting
Introduction to Regulatory Affairs for Biotech
An Introduction to Immunogenicity
The Pharma Executive Mini-MBA
EU Pharmaceutical Law
Regulatory Affairs for Biotech
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