Welcome. If you're a registered user, please
log-in.
If not, please
sign-up
.
email:
registration@pti-europe.co.uk
phone:
+44 (0) 20 7017 7481
GO
Immunogenicity
22 May 2013
Download Event Programme
Subscribe to e-Mail or SMS Alerts
Where am I?
PTI
>
Immunogenicity
> Feeds
Subscribe to RSS feed updates for
Immunogenicity here
Subscribe to RSS feed updates for PTI events
Biomarkers
Registering Agrochemicals in the EU
Mastering Regulatory and Development Strategies for Generics
EU Pharmaceutical Law
Show feeds from other topic areas here
Subscribe to RSS feed updates for Agrochemical events
Agrochemical Off-Patent and Generic Products: Registrations and Regulations as means to market development
Patent Law and Practice in Agrochemicals
Regulatory Affairs for Biopesticides
Subscribe to RSS feed updates for Biopharmaceuticals events
Comparability for Biologics
An Introduction to Immunogenicity
Protecting Inventions in the Biotech Industry
Analysing and Validating Biological Assays
EU Biosimilar Registration and Marketing Requirements
Antibody Display, Selection and Engineering
CMC Analytical, Comparability and Stability Studies for Biotechnology Products
Regulatory Affairs for Biotech
Subscribe to RSS feed updates for Clinical events
Regulatory Affairs for Clinical Trials
Risk-Based Monitoring & Targeted SDV
Best Practice for Clinical Monitors and CRAs
Management of Product Development in Healthcare
CRO Contracts
Clinical Research Project Management
Budget Management for Clinical Trials
Effectively Managing Vendor Oversight
Subscribe to RSS feed updates for Manufacturing events
A Practical Guide to Biopharmaceutical Manufacturing
Stability Testing for Pharmaceuticals
Subscribe to RSS feed updates for R & D events
Practical solutions for establishing in vitro-in vivo correlation
Pharmaceutical Licensing
An Introduction to Pharmacoeconomics
Introduction to Pharmacokinetics for the Non-Specialist
Advanced Toxicology
How Drugs Are Developed
Introduction to Toxicology for the Non-specialist
Intermediate Pharmacokinetics
Genotoxic Impurities– Strategies for Identification and Control
Subscribe to RSS feed updates for Animal Health events
Regulatory Affairs for Veterinary Medicines
The Regulation of Veterinary Medicine
Subscribe to RSS feed updates for Business Strategy events
Pharma Executive Mini-MBA
Subscribe to RSS feed updates for Fine Chemicals events
Dossier Preparation for Biocides
Subscribe to RSS feed updates for Medical Devices & Diagnostics events
Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
Medical Device School
Conducting Medical Device Trials in the EU
Conducting Medical Device Trials in the US
Patent Law and Practice in Medical Devices
Introduction to Regulatory Affairs for Medical Devices
Advanced Regulatory Affairs for Medical Devices
Subscribe to RSS feed updates for Regulatory Affairs events
A Practical Guide to Pharmacovigilance and Drug Safety
Pharmaceutical Regulatory Affairs in the EU and US
Dissolution Testing
Building the eCTD
Understanding and Preparing the Quality and Pharmaceutical Module of the Global CTD Dossier
Patent Law and Practice in Pharmaceuticals
Advanced European Regulatory Affairs
Filing Variations
Signal Detection Strategies
Introduction to European Regulatory Affairs
US-FDA Drug Submission Procedures
An Introduction to Pharmacovigilance
Intermediate Pharmacovigilance and Adverse Event Reporting
Gaining Marketing Authorisations in CIS
EU and US Requirements for Pharmaceutical Labelling & Package Leaflets
Pharmaceutical Regulatory Affairs in China
Introduction to Regulatory Affairs for Biotech
Conducting Paediatric Clinical Trials
Regulatory Affairs Strategies
Website navigation:
Home
About Us
Dates/Venue
Who Should Attend
Your Course Leader
Contact us
Other Training Courses
Past Attendee Comments
Website Secondary navigation:
IIR Home
Would you like to be a Speaker/Trainer?
Tailored Training Solutions
Accommodation