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Upcoming Courses

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May 2012
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Introduction to Regulatory Affairs for Biotech

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

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

Building the eCTD
22 - 23 May 2012
MWB Victoria

Building the eCTD

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Understanding and Preparing the Quality and Pharmaceutical Module of the Global CTD Dossier

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

Medical Device School
22 - 24 May 2012
London

Medical Device School

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June 2012
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Analysing Biological Assays

Analysing Biological Assays
11 - 12 June 2012
Regent, Berlin, Germany

Analysing Biological Assays

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Gaining Marketing Authorisations in CIS

Gaining Marketing Authorisations in CIS
13 - 14 June 2012
MWB Victoria

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Conducting Paediatric Clinical Trials

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

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

Introduction to European Regulatory Affairs
19 - 21 June 2012
Regus Princeton - Forrestal Village, New Jersey, USA

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CRO Contracts

CRO Contracts
19 - 20 June 2012
MWB Victoria

CRO Contracts

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Advanced European Regulatory Affairs

Advanced European Regulatory Affairs
26 - 28 June 2012
MWB Victoria

Advanced European Regulatory Affairs

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Effectively Managing Vendor Oversight

Effectively Managing Vendor Oversight
26 - 27 June 2012
MWB Victoria

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CMC Analytical, Comparability and Stability Studies for Biotechnology and Biosimilar Products

CMC Analytical, Comparability and Stability Studies for ...
26 - 27 June 2012
Regus Princeton - Forrestal Village, New Jersey, USA

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European Regulatory Affairs School

European Regulatory Affairs School
27 - 29 June 2012
London

European Regulatory Affairs School

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Introduction to Regulatory Affairs for Medical Devices

Introduction to Regulatory Affairs for Medical Devices
27 - 28 June 2012
MWB Victoria

Introduction to Regulatory Affairs for Medical Devices

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July 2012
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Registering Agrochemicals in the EU

Registering Agrochemicals in the EU
2 - 3 July 2012
MWB Edinburgh

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Bioanalytical School

Bioanalytical School
3 - 5 July 2012
MWB Edinburgh

Bioanalytical School

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EU Pharmaceutical Law

EU Pharmaceutical Law
3 - 5 July 2012
The Roxburghe Hotel Edinburgh

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Intermediate Level Adverse Event Reporting

Intermediate Level Adverse Event Reporting
4 - 5 July 2012
MWB Edinburgh

Intermediate Level Adverse Event Reporting

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Clinical Research Project Management

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

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

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

Dissolution Testing
10 - 11 July 2012
NH Amsterdam Centre

Dissolution Testing

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Mastering Regulatory and Development Strategies for Generics

Mastering Regulatory and Development Strategies for Generics
11 - 12 July 2012
MWB Edinburgh

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Regulatory Affairs for Biotech

Regulatory Affairs for Biotech
17 - 18 July 2012
Regus Boston Independence Wharf, Boston, USA

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Budget Management for Clinical Trials

Budget Management for Clinical Trials
17 - 18 July 2012
MWB Edinburgh

Budget Management for Clinical Trials

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Project Management for Clinical Trials

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

Filing Variations
19 - 20 July 2012
Kempinski Hotel Bristol, Berlin

Filing Variations

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Adverse Event Reporting & Pharmacovigilance

Adverse Event Reporting & Pharmacovigilance
24 - 25 July 2012
Hotel le Plaza, Brussels, Belgium

Adverse Event Reporting & Pharmacovigilance

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August 2012
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Practical solutions for establishing in vitro-in vivo correlation

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

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

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

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

Mastering your Performance as a QA Professional
22 - 23 August 2012
REGUS, One Embarcadero, San Francisco, USA

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Biomarkers

Biomarkers
22 - 23 August 2012
MWB Cambridge

Biomarkers

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Writing Standard Operating Procedures

Writing Standard Operating Procedures
23 - 24 August 2012
Regus Soma- San Francisco, California, USA

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September 2012
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CMC Analytical, Comparability and Stability Studies for Biotechnology and Biosimilar Products

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

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

Scientific Advice
6 - 7 September 2012
MWB Edinburgh

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Genotoxic Impurities– Strategies for Identification and Control

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

Successful Strategies for Monitoring Clinical Trials
10 - 11 September 2012
MWB Victoria

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Effectively Managing Vendor Oversight

Effectively Managing Vendor Oversight
11 - 12 September 2012
MWB Victoria

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US-FDA Drug Submission Procedures

US-FDA Drug Submission Procedures
11 - 12 September 2012
MWB Victoria

US-FDA Drug Submission Procedures

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Analysing Biological Assays

Analysing Biological Assays
12 - 13 September 2012
MWB Victoria

Analysing Biological Assays

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Adverse Event Reporting & Pharmacovigilance

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

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

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

Building the eCTD
19 - 20 September 2012
MWB Victoria

Building the eCTD

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Auditing Clinical Trials for GCP Compliance

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 Vigilance Reporting

Successful Medical Device & IVD Post Market Surveillance and...
19 - 20 September 2012
MWB Victoria

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Introduction to Good Manufacturing Practices (GMPs)

Introduction to Good Manufacturing Practices (GMPs)
20 - 21 September 2012
REGUS Overlook Princeton, New Jersey, USA

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Regulatory Affairs Strategies

Regulatory Affairs Strategies
20 - 21 September 2012
MWB Victoria

Regulatory Affairs Strategies

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Regulatory Affairs for Clinical Trials

Regulatory Affairs for Clinical Trials
27 - 28 September 2012
MWB Victoria

Regulatory Affairs for Clinical Trials

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October 2012
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Regulatory Affairs for Veterinary Medicines

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

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

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

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 Module of the Global CTD Dossier

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

CRO Contracts
16 - 17 October 2012
MWB Victoria

CRO Contracts

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Medical Device School

Medical Device School
16 - 18 October 2012
London

Medical Device School

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Gaining Marketing Authorisations in CIS

Gaining Marketing Authorisations in CIS
17 - 18 October 2012
Renaissance Polat Istanbul Hotel

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IMMUNOGENICITY

Immunogenicity
17 - 18 October 2012
Regus Soma- San Francisco, California, USA

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Introduction to European Regulatory Affairs

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

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

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 Biotechnology Products

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

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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November 2012
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Mastering EU Requirements for Product Labelling and Package Leaflets

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

Bioanalytical School
6 - 8 November 2012
MWB Victoria

Bioanalytical School

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Dissolution Testing

Dissolution Testing
6 - 7 November 2012
MWB Victoria

Dissolution Testing

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Advanced Toxicology

Advanced Toxicology
6 - 8 November 2012
MWB Victoria

Advanced Toxicology

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Biomarkers

Biomarkers
8 - 9 November 2012
MWB Victoria

Biomarkers

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Biocidal Products Directive (98/8/EC)

Biocidal Products Directive (98/8/EC)
8 - 9 November 2012
MWB Victoria

Biocidal Products Directive (98/8/EC)

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The Pharma Executive Mini-MBA

Pharma Executive Mini-MBA
12 - 16 November 2012
The Rubens Hotel, London, UK

The Pharma Executive Mini-MBA

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Intermediate Pharmacokinetics

Intermediate Pharmacokinetics
13 - 14 November 2012
MWB Victoria

Intermediate Pharmacokinetics

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Registering Agrochemicals in the EU

Registering Agrochemicals in the EU
14 - 15 November 2012
MWB Victoria

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Writing and Managing SOPs for Clinical Quality Assurance

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

Regulatory Affairs for Biotech
15 - 16 November 2012
MWB Victoria

Regulatory Affairs for Biotech

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Filing Variations

Filing Variations
15 - 16 November 2012
MWB Victoria

Filing Variations

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Regulatory Affairs for Biotech

Regulatory Affairs for Biotech
27 - 28 November 2012
Regus Mission Valley, San Diego, California, USA

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Clinical Research Project Management

Clinical Research Project Management
27 - 29 November 2012
MWB Victoria

Clinical Research Project Management

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Genotoxic Impurities– Strategies for Identification and Control

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

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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December 2012
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Writing Standard Operating Procedures

Writing Standard Operating Procedures
3 - 4 December 2012
Regus Soma- San Francisco, California, USA

More Info
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Adverse Event Reporting & Pharmacovigilance

Adverse Event Reporting & Pharmacovigilance
4 - 5 December 2012
MWB Victoria

Adverse Event Reporting & Pharmacovigilance

More Info
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Mastering Your Performance as a QA Professional

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

Introduction to Pharmacokinetics for the Non-Specialist
4 - 5 December 2012
Hotel le Plaza, Brussels, Belgium

Introduction to Pharmacokinetics for the Non-Specialist

More Info
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Introduction to Toxicology for the Non-specialist

Introduction to Toxicology for the Non-specialist
4 - 5 December 2012
MWB Victoria

Introduction to Toxicology for the Non-specialist

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Intermediate Level Adverse Event Reporting

Intermediate Level Adverse Event Reporting
6 - 7 December 2012
MWB Victoria

Intermediate Level Adverse Event Reporting

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Effectively Managing Vendor Oversight

Effectively Managing Vendor Oversight
6 - 7 December 2012
Regus Soma- San Francisco, California, USA

More Info
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Budget Management for Clinical Trials

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 correlation

Practical solutions for establishing in vitro-in vivo ...
11 - 12 December 2012
MWB Victoria

More Info
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Conducting Paediatric Clinical Trials

Conducting Paediatric Clinical Trials
13 - 14 December 2012
MWB Victoria

Conducting Paediatric Clinical Trials

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Past Courses

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November 2011
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Signal Detection Strategies
8 - 9 November 2011
MWB Victoria
More Info

Analytical Data at the Service of QA, Regulatory and ...
21 - 22 November 2011
MWB Victoria
More Info

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February 2012
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Advanced European Regulatory Affairs
21 - 23 February 2012
MWB Victoria
More Info

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March 2012
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April 2012
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Comparability for Biologics
17 - 18 April 2012
MWB Victoria
More Info

Introduction to European Regulatory Affairs
17 - 19 April 2012
Renaissance Zurich Hotel
More Info

Regulatory Affairs for Clinical Trials
23 - 24 April 2012
MWB Victoria
More Info

An Introduction to Immunogenicity
26 - 27 April 2012
MWB Victoria
More Info

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May 2012
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Successful Medical Device & IVD Post Market Surveillance and...
10 - 11 May 2012
etc. venues Victoria
More Info

Auditing Clinical Trials for GCP Compliance
15 - 16 May 2012
Regus Boston Independence Wharf, Boston, USA
More Info

Biocidal Products Directive (98/8/EC)
15 - 16 May 2012
MWB Victoria
More Info

Introduction to Good Manufacturing Practices (GMPs)
16 - 17 May 2012
Regus Boston Independence Wharf, Boston, USA
More Info

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