- email:registration@pti-europe.co.uk
- phone:+44 (0) 20 7017 7481
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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
Clinical Research Project Management
"I am new in Project Management. Very helpful and explained the basics needed"
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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Introduction to Pharmacokinetics for the Non-Specialist
22 - 23 May 2012
MWB Victoria
Introduction to Pharmacokinetics for the Non-Specialist
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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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Medical Device School
22 - 24 May 2012
London
Medical Device School
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Analysing Biological Assays
11 - 12 June 2012
Regent, Berlin, Germany
Analysing Biological Assays
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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 Toxicology for the Non-specialist
19 - 20 June 2012
Hotel le Plaza, Brussels, Belgium
Introduction to Toxicology for the Non-specialist
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Introduction to European Regulatory Affairs
19 - 21 June 2012
Regus Princeton - Forrestal Village, New Jersey, USA
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CRO Contracts
19 - 20 June 2012
MWB Victoria
CRO Contracts
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Advanced European Regulatory Affairs
26 - 28 June 2012
MWB Victoria
Advanced European Regulatory Affairs
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Effectively Managing Vendor Oversight
26 - 27 June 2012
MWB Victoria
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CMC Analytical, Comparability and Stability Studies for ...
26 - 27 June 2012
Regus Princeton - Forrestal Village, New Jersey, USA
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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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Bioanalytical School
3 - 5 July 2012
MWB Edinburgh
Bioanalytical School
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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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Clinical Research Project Management
4 - 6 July 2012
MWB Edinburgh
Clinical Research Project Management
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QA and QC Compliance Strategies for Biopharmaceuticals
5 - 6 July 2012
MWB Edinburgh
QA and QC Compliance Strategies for Biopharmaceuticals
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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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Budget Management for Clinical Trials
17 - 18 July 2012
MWB Edinburgh
Budget Management for Clinical Trials
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Fundamentals of
Project Management
Commences: Tuesday 17th July 2012
How to initiate, plan and implement successful projects
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Project Management for Clinical Trials
18 - 19 July 2012
REGUS Boston Prudential Tower, Boston, USA
Project Management for Clinical Trials
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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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Effectively Managing Vendor Oversight
21 - 22 August 2012
Regus Soma- San Francisco, California, USA
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Introduction to Pharmacokinetics for the Non-Specialist
21 - 22 August 2012
MWB Cambridge
Introduction to Pharmacokinetics for the Non-Specialist
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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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CMC Analytical, Comparability and Stability Studies for ...
5 - 6 September 2012
Regus Boston Independence Wharf, Boston, USA
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Antibody Display, Selection and Engineering
5 - 6 September 2012
Hotel le Plaza, Brussels, Belgium
Antibody Display, Selection and Engineering
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Scientific Advice
6 - 7 September 2012
MWB Edinburgh
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Genotoxic Impurities– Strategies for Identification and ...
6 - 7 September 2012
Hotel le Plaza, Brussels, Belgium
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Successful Strategies for Monitoring Clinical Trials
10 - 11 September 2012
MWB Victoria
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Effectively Managing Vendor Oversight
11 - 12 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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Analysing Biological Assays
12 - 13 September 2012
MWB Victoria
Analysing Biological Assays
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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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Introduction to Toxicology for the Non-specialist
18 - 19 September 2012
MWB Victoria
Introduction to Toxicology for the Non-specialist
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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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Successful Medical Device & IVD Post Market Surveillance and...
19 - 20 September 2012
MWB Victoria
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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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QA and QC Compliance Strategies for Biopharmaceuticals
11 - 12 October 2012
MWB Victoria
QA and QC Compliance Strategies for Biopharmaceuticals
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Small Molecule Drug Discovery
15 - 16 October 2012
MWB Victoria
Small Molecule Drug Discovery
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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
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CRO Contracts
16 - 17 October 2012
MWB Victoria
CRO Contracts
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Medical Device School
16 - 18 October 2012
London
Medical Device School
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Gaining Marketing Authorisations in CIS
17 - 18 October 2012
Renaissance Polat Istanbul Hotel
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Immunogenicity
17 - 18 October 2012
Regus Soma- San Francisco, California, USA
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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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CMC Analytical, Comparability and Stability Studies for ...
24 - 25 October 2012
MWB Victoria
CMC Analytical, Comparability and Stability Studies for Biotechnology Products
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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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Bioanalytical School
6 - 8 November 2012
MWB Victoria
Bioanalytical School
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Dissolution Testing
6 - 7 November 2012
MWB Victoria
Dissolution Testing
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Advanced Toxicology
6 - 8 November 2012
MWB Victoria
Advanced Toxicology
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Biomarkers
8 - 9 November 2012
MWB Victoria
Biomarkers
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Biocidal Products Directive (98/8/EC)
8 - 9 November 2012
MWB Victoria
Biocidal Products Directive (98/8/EC)
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Pharma Executive Mini-MBA
12 - 16 November 2012
The Rubens Hotel, London, UK
The Pharma Executive Mini-MBA
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Intermediate Pharmacokinetics
13 - 14 November 2012
MWB Victoria
Intermediate Pharmacokinetics
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Registering Agrochemicals in the EU
14 - 15 November 2012
MWB Victoria
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Writing and Managing SOPs for Clinical Quality Assurance
15 - 16 November 2012
MWB Victoria
Writing and Managing SOPs for Clinical Quality Assurance
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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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Clinical Research Project Management
27 - 29 November 2012
MWB Victoria
Clinical Research Project Management
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Genotoxic Impurities– Strategies for Identification and ...
28 - 29 November 2012
REGUS Emerald Plaza, San Diego, USA
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Project Management for Clinical Trials
29 - 30 November 2012
Regus Mission Valley, San Diego, California, USA
Project Management for Clinical Trials
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Writing Standard Operating Procedures
3 - 4 December 2012
Regus Soma- San Francisco, California, USA
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Adverse Event Reporting & Pharmacovigilance
4 - 5 December 2012
MWB Victoria
Adverse Event Reporting & Pharmacovigilance
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Mastering your Performance as a QA Professional
4 - 5 December 2012
REGUS, One Embarcadero, San Francisco, USA
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Introduction to Pharmacokinetics for the Non-Specialist
4 - 5 December 2012
Hotel le Plaza, Brussels, Belgium
Introduction to Pharmacokinetics for the Non-Specialist
More InfoDownload Latest Programme
Register for this Course
Introduction to Toxicology for the Non-specialist
4 - 5 December 2012
MWB Victoria
Introduction to Toxicology for the Non-specialist
More InfoDownload Latest Programme
Register for this Course
Intermediate Level Adverse Event Reporting
6 - 7 December 2012
MWB Victoria
Intermediate Level Adverse Event Reporting
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Effectively Managing Vendor Oversight
6 - 7 December 2012
Regus Soma- San Francisco, California, USA
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Budget Management for Clinical Trials
6 - 7 December 2012
MWB Victoria
Budget Management for Clinical Trials
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Practical solutions for establishing in vitro-in vivo ...
11 - 12 December 2012
MWB Victoria
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Conducting Paediatric Clinical Trials
13 - 14 December 2012
MWB Victoria
Conducting Paediatric Clinical Trials
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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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How Drugs Are Developed
ongoing self study course
self-study course
How Drugs Are Developed
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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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Pharmaceutical Licensing
ongoing self study course
self-study course
Pharmaceutical Licensing
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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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Effective Project Management in Drug Development
ongoing self-study course
self study course
Effective Project Management in Drug Development
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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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Stability Testing for Pharmaceuticals
ongoing self-study course
self-study course
Stability Testing for Pharmaceuticals
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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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Analytical Data at the Service of QA, Regulatory and ...
21 - 22 November 2011
MWB Victoria
More Info..
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CMC Analytical, Comparability and Stability Studies for ...
14 - 15 March 2012
MWB Victoria
More Info..
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Successful Medical Device & IVD Post Market Surveillance and...
10 - 11 May 2012
etc. venues Victoria
More InfoAuditing 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..