- email:registration@pti-europe.co.uk
- phone:+44 (0) 20 7017 7481
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CPD Points
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.
Reviews
Writing and Managing SOPs for Clinical Quality Assurance
"Excellent course. Good balance between slide presentation, exercises and interaction"
European Regulatory Affairs School
"Really good overview of all aspects of RA. Although I’ve been in this business for some time, it was a good opportunity to learn about coming changes in certain procedures. Also to exchange experiences with colleagues from other countries and companies."
Accommodation
Need Accommodation? PTI has arranged a special room rate with Hotel Map at a number of hotels.
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Upcoming Courses
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Introduction to Regulatory Affairs for Biotech
22 - 24 May 2012
MWB Victoria
Introduction to Regulatory Affairs for Biotech
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Building the eCTD
22 - 23 May 2012
MWB Victoria
Building the eCTD
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Understanding and Preparing the Quality and Pharmaceutical ...
22 - 24 May 2012
Green Park Hilton
Understanding and Preparing the Quality and Pharmaceutical Module of the Global CTD Dossier
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Gaining Marketing Authorisations in CIS
13 - 14 June 2012
MWB Victoria
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Conducting Paediatric Clinical Trials
13 - 14 June 2012
MWB Victoria
Conducting Paediatric Clinical Trials
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Introduction to European Regulatory Affairs
19 - 21 June 2012
Regus Princeton - Forrestal Village, New Jersey, USA
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Advanced European Regulatory Affairs
26 - 28 June 2012
MWB Victoria
Advanced European Regulatory Affairs
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IBC Legal's
REACH: Legal Implications & Supply Chain Strategies 2012
26 - 27 June 2012
Hotel Metropole, Brussels
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European Regulatory Affairs School
27 - 29 June 2012
London
European Regulatory Affairs School
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Introduction to Regulatory Affairs for Medical Devices
27 - 28 June 2012
MWB Victoria
Introduction to Regulatory Affairs for Medical Devices
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Registering Agrochemicals in the EU
2 - 3 July 2012
MWB Edinburgh
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EU Pharmaceutical Law
3 - 5 July 2012
The Roxburghe Hotel Edinburgh
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Intermediate Level Adverse Event Reporting
4 - 5 July 2012
MWB Edinburgh
Intermediate Level Adverse Event Reporting
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The European Chemicals Policy - REACH
9 - 10 July 2012
Regus Princeton - Forrestal Village, New Jersey, USA
The European Chemicals Policy - REACH
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Dissolution Testing
10 - 11 July 2012
NH Amsterdam Centre
Dissolution Testing
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Mastering Regulatory and Development Strategies for Generics
11 - 12 July 2012
MWB Edinburgh
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Regulatory Affairs for Biotech
17 - 18 July 2012
Regus Boston Independence Wharf, Boston, USA
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Filing Variations
19 - 20 July 2012
Kempinski Hotel Bristol, Berlin
Filing Variations
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Adverse Event Reporting & Pharmacovigilance
24 - 25 July 2012
Hotel le Plaza, Brussels, Belgium
Adverse Event Reporting & Pharmacovigilance
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Practical solutions for establishing in vitro-in vivo ...
7 - 8 August 2012
Andel's Hotel & Suites, Prague
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Introduction to European Regulatory Affairs
21 - 23 August 2012
MWB Cambridge
Introduction to European Regulatory Affairs
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Mastering your Performance as a QA Professional
22 - 23 August 2012
REGUS, One Embarcadero, San Francisco, USA
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Biomarkers
22 - 23 August 2012
MWB Cambridge
Biomarkers
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Writing Standard Operating Procedures
23 - 24 August 2012
Regus Soma- San Francisco, California, USA
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Scientific Advice
6 - 7 September 2012
MWB Edinburgh
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Successful Strategies for Monitoring Clinical Trials
10 - 11 September 2012
MWB Victoria
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US-FDA Drug Submission Procedures
11 - 12 September 2012
MWB Victoria
US-FDA Drug Submission Procedures
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Adverse Event Reporting & Pharmacovigilance
13 - 14 September 2012
MWB Victoria
Adverse Event Reporting & Pharmacovigilance
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Introduction to Regulatory Affairs for Medical Devices
18 - 19 September 2012
MWB Victoria
Introduction to Regulatory Affairs for Medical Devices
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Building the eCTD
19 - 20 September 2012
MWB Victoria
Building the eCTD
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Auditing Clinical Trials for GCP Compliance
19 - 20 September 2012
Regus Princeton - Forrestal Village, New Jersey, USA
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Introduction to Good Manufacturing Practices (GMPs)
20 - 21 September 2012
REGUS Overlook Princeton, New Jersey, USA
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Regulatory Affairs Strategies
20 - 21 September 2012
MWB Victoria
Regulatory Affairs Strategies
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Regulatory Affairs for Clinical Trials
27 - 28 September 2012
MWB Victoria
Regulatory Affairs for Clinical Trials
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Regulatory Affairs for Veterinary Medicines
9 - 10 October 2012
MWB Victoria
Regulatory Affairs for Veterinary Medicines
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Registration of Pharmaceuticals in the EU
9 - 11 October 2012
MWB Victoria
Registration of Pharmaceuticals in the EU
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Understanding and Preparing the Quality and Pharmaceutical ...
16 - 18 October 2012
Hotel le Plaza, Brussels, Belgium
Understanding and Preparing the Quality and Pharmaceutical Module of the Global CTD Dossier
More InfoDownload Latest Programme
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Gaining Marketing Authorisations in CIS
17 - 18 October 2012
Renaissance Polat Istanbul Hotel
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Introduction to European Regulatory Affairs
17 - 19 October 2012
REGUS Boston Prudential Tower, Boston, USA
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Regulatory Affairs for Preclinical Safety Studies
18 - 19 October 2012
MWB Victoria
Regulatory Affairs for Preclinical Safety Studies
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Advanced European Regulatory Affairs
23 - 25 October 2012
MWB Victoria
Advanced European Regulatory Affairs
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The European Chemicals Policy - REACH
29 - 30 October 2012
Regus Mission Valley, San Diego, California, USA
The European Chemicals Policy - REACH
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Mastering EU Requirements for Product Labelling and Package ...
6 - 8 November 2012
MWB Victoria
Mastering EU Requirements for Product Labelling and Package Leaflets
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Dissolution Testing
6 - 7 November 2012
MWB Victoria
Dissolution Testing
More InfoDownload Latest Programme
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Biomarkers
8 - 9 November 2012
MWB Victoria
Biomarkers
More InfoDownload Latest Programme
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Registering Agrochemicals in the EU
14 - 15 November 2012
MWB Victoria
More InfoDownload Latest Programme
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Regulatory Affairs for Biotech
15 - 16 November 2012
MWB Victoria
Regulatory Affairs for Biotech
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Filing Variations
15 - 16 November 2012
MWB Victoria
Filing Variations
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Regulatory Affairs for Biotech
27 - 28 November 2012
Regus Mission Valley, San Diego, California, USA
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Writing Standard Operating Procedures
3 - 4 December 2012
Regus Soma- San Francisco, California, USA
More InfoDownload Latest Programme
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Adverse Event Reporting & Pharmacovigilance
4 - 5 December 2012
MWB Victoria
Adverse Event Reporting & Pharmacovigilance
More InfoDownload Latest Programme
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Mastering your Performance as a QA Professional
4 - 5 December 2012
REGUS, One Embarcadero, San Francisco, USA
More InfoDownload Latest Programme
Register for this Course
Intermediate Level Adverse Event Reporting
6 - 7 December 2012
MWB Victoria
Intermediate Level Adverse Event Reporting
More InfoDownload Latest Programme
Register for this Course
Practical solutions for establishing in vitro-in vivo ...
11 - 12 December 2012
MWB Victoria
More InfoDownload Latest Programme
Register for this Course
Conducting Paediatric Clinical Trials
13 - 14 December 2012
MWB Victoria
Conducting Paediatric Clinical Trials
More InfoDownload Latest Programme
Register for this Course
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A Practical Guide to Pharmacovigilance and Drug Safety
ongoing self study course
self study course
A Practical Guide to Pharmacovigilance and Drug Safety
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Pharmaceutical Regulatory Affairs in the EU and US
Ongoing self study course
self study course
Pharmaceutical Regulatory Affairs in the EU and US
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Conduction Medical Device Trials in the EU
A 10 week self study course
self-study course
Conduction Medical Device Trials in the EU
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A Practical Guide to Biopharmaceutical Manufacturing
ongoing self study course
self-study course
A Practical Guide to Biopharmaceutical Manufacturing
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An Introduction to Pharmacoeconomics
ongoing self-study course
self-study course
An Introduction to Pharmacoeconomics
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Conducting Medical Device Trials in the US
Ongoing self-study course
self-study course
Conducting Medical Device Trials in the US
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Patent Law and Practice in Medical Devices
10 Week self study course
self study course
Patent Law and Practice in Medical Devices
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Patent Law and Practice in Pharmaceuticals
10 Week self study course
self study course
Patent Law and Practice in Pharmaceuticals
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The Regulation of Veterinary Medicine
ongoing self-study course
self study course
The Regulation of Veterinary Medicine
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Patent Law and Practice in Agrochemicals
ongoing self study course
self study course
Patent Law and Practice in Agrochemicals
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Protecting Inventions in the Biotech Industry
Ongoing self study course
self-study course
Protecting Inventions in the Biotech Industry
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Past Courses
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Auditing Clinical Trials for GCP Compliance
15 - 16 May 2012
Regus Boston Independence Wharf, Boston, USA
More InfoIntroduction to Good Manufacturing Practices (GMPs)
16 - 17 May 2012
Regus Boston Independence Wharf, Boston, USA
More Info..