Regus Victoria - Upcoming.org Archive

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August 12, 2007

Project Management in the Generics Industry at Regus Victoria

August 14, 2007

Introduction to European Regulatory Affairs at Regus Victoria

September 3, 2007

Filing Variations at Regus Victoria

September 9, 2007

Understanding US-FDA Drug Submission Procedures at Regus Victoria

September 9, 2007

Introduction to Pharmacokinetics for the Non-specialist at Regus Victoria

September 12, 2007

FDA Requirements for Packaging and Labelling at Regus Victoria

September 16, 2007

Analysing Biological Assays at Regus Victoria

September 19, 2007

Introduction to Pharmaceutical Patents at Regus Victoria

September 26, 2007

Scientific Advice at Regus Victoria

October 2, 2007

Mastering EU Requirements for Product Labelling & Package Leaflets at Regus Victoria

October 3, 2007

Regulatory Affairs for Veterinary Medicines at Regus Victoria

October 7, 2007

Devising Successful CRO Contracts at Regus Victoria

October 15, 2007

Advanced Pharmacokinetics at Regus Victoria

October 22, 2007

Regulatory Affairs for Generics at Regus Victoria

November 4, 2007

Introduction to Regulatory Affairs for Biotech at Regus Victoria

November 5, 2007

Building the eCTD at Regus Victoria

November 5, 2007

Regulatory Affairs for Combination products at Regus Victoria

November 7, 2007

Regulatory Affairs for Biotechnology at Regus Victoria

November 12, 2007

Qualified Person in Clinical Trials at Regus Victoria

November 18, 2007

Adverse Event Reporting and Pharmacovigilance at Regus Victoria

November 20, 2007

Advanced-level Adverse Event Reporting & Pharmacovigilance at Regus Victoria

November 26, 2007

Dissolution Testing at Regus Victoria

November 28, 2007

Signal Detection Strategies at Regus Victoria

December 2, 2007

Introduction to Pharmaceutical Patents at Regus Victoria

December 2, 2007

Introduction to pharmacokinetics for the non-specialist at Regus Victoria

December 4, 2007

Comparability for Biologics at Regus Victoria

December 4, 2007

Advanced Pharmacokinetics at Regus Victoria

December 5, 2007

Developing Global Pharmaceutical Pricing Strategies at Regus Victoria

December 5, 2007

Filing Variations at Regus Victoria

December 10, 2007

Introduction to Toxicology for the Non-specialist at Regus Victoria

January 16, 2008

Scientific Advice at Regus Victoria

January 20, 2008

Analysing Biological Assays at Regus Victoria

January 23, 2008

Regulatory Affairs for Veterinary Medicines at Regus Victoria

January 23, 2008

Introduction to Immunogenicity at Regus Victoria

January 23, 2008

Introduction to Immunogenicity (Cancelled) at Regus Victoria

February 4, 2008

Advanced European Regulatory Affairs at Regus Victoria

February 6, 2008

Biocidal Products Directive at Regus Victoria

February 10, 2008

Antibody Display, Selection and Engineering at Regus Victoria

February 18, 2008

Introduction to Toxicology for the Non-specialist at Regus Victoria

February 18, 2008

Preparing the Chemistry and Pharmacy Section of the EU Registration Dossier at Regus Victoria

February 24, 2008

Devising Successful CRO Contracts at Regus Victoria

February 27, 2008

Regulatory Affairs for Generics at Regus Victoria

March 3, 2008

Filing Variations at Regus Victoria

March 4, 2008

Stability Testing for Biotechnology Products at Regus Victoria

March 5, 2008

Veterinary Clinical Trials at Regus Victoria

March 5, 2008

Introduction to Regulatory Affairs for Biotech at Regus Victoria

March 5, 2008

Introduction to pharmacokinetics for the non-specialist at Regus Victoria

March 9, 2008

Mastering EU Requirements for Product Labelling & Package Leaflets at Regus Victoria

March 12, 2008

Regulatory Affairs for Biotechnology at Regus Victoria

March 17, 2008

Regulatory Affairs for Combination products at Regus Victoria

March 17, 2008

Regulatory Affairs for Phase I Clinical Trials at Regus Victoria

March 25, 2008

Dissolution Testing at Regus Victoria

March 25, 2008

Environmental Risk Assessment of Human Pharmaceuticals at Regus Victoria

March 30, 2008

Understanding US-FDA Drug Submission Procedures at Regus Victoria

March 31, 2008

Adverse Event Reporting and Pharmacovigilance at Regus Victoria

April 9, 2008

The European Chemicals Policy - REACH at Regus Victoria

April 13, 2008

Project Management in the Generics Industry at Regus Victoria

April 21, 2008

Building the eCTD at Regus Victoria

April 23, 2008

Advanced-level Adverse Event Reporting & Pharmacovigilance at Regus Victoria

April 28, 2008

Budget Management for Clinical Trials at Regus Victoria

April 28, 2008

Comparability for Biologics at Regus Victoria

April 28, 2008

Toxicology at Regus Victoria

April 28, 2008

Conducting Paediatric Clinical Trials at Regus Victoria

May 5, 2008

Antibody Display, Selection and Engineering at Regus Victoria

May 7, 2008

Introduction to Immunogenicity at Regus Victoria

May 15, 2008

Securing US Reimbursement for Medical Devices at Regus Victoria

June 1, 2008

Advanced European Regulatory Affairs at Regus Victoria

June 3, 2008

Environmental Risk Assessment of Human Pharmaceuticals at Regus Victoria

June 4, 2008

Devising Successful CRO Contracts at Regus Victoria

June 8, 2008

Mastering EU Requirements for Product Labelling & Package Leaflets at Regus Victoria

June 18, 2008

Regulatory Affairs for Biotechnology at Regus Victoria

June 22, 2008

Veterinary Clinical Trials at Regus Victoria

June 22, 2008

Introduction to European Regulatory Affairs at Regus Victoria

June 24, 2008

Stability Testing for Biotechnology Products at Regus Victoria

June 25, 2008

Regulatory Affairs for Combination Products at Regus Victoria

June 30, 2008

Biocidal Products Directive at Regus Victoria

July 1, 2008

Clinical Research Project Management at Regus Victoria

July 2, 2008

Conducting Paediatric Clinical Trials at Regus Victoria

July 2, 2008

Regulatory Affairs Strategies at Regus Victoria

July 6, 2008

Introduction to Regulatory Affairs for Biotech at Regus Victoria

July 15, 2008

Dissolution Testing at Regus Victoria

July 21, 2008

Introduction to Toxicology for the Non-Specialist at Regus Victoria

July 27, 2008

Regulatory Affairs for Phase I Clinical Trials at Regus Victoria

August 4, 2008

Introduction to Pharmaceutical Patents at Regus Victoria

August 4, 2008

Introduction to Pharmacokinetics for the Non-Specialist at Regus Victoria

August 17, 2008

Project Management in the Generics Industry at Regus Victoria

August 17, 2008

The European Chemicals Policy - REACH at Regus Victoria

August 26, 2008

Preparing the Chemistry and Pharmacy Section of the EU Registration Dossier at Regus Victoria

August 27, 2008

Budget Management for Clinical Trials at Regus Victoria

August 27, 2008

Cleaning Validation at Regus Victoria

August 31, 2008

Adverse Event Reporting and Pharmacovigilance at Regus Victoria

September 3, 2008

Advanced-Level Adverse Event Reporting & Pharmacovigilance at Regus Victoria

September 7, 2008

Analysing Biological Assays at Regus Victoria

September 10, 2008

Scientific Advice at Regus Victoria

September 16, 2008

Antibody Display, Selection and Engineering at Regus Victoria

September 28, 2008

Introduction to Immunogenicity at Regus Victoria

October 1, 2008

Introduction to Regulatory Affairs for Medical Devices at Regus Victoria

October 1, 2008

Regulatory Affairs for Veterinary Medicines at Regus Victoria

October 6, 2008

Advanced European Regulatory Affairs at Regus Victoria

October 15, 2008

Securing US Reimbursement for Medical Devices at Regus Victoria

October 19, 2008

Introduction to Regulatory Affairs for Biotech at Regus Victoria

October 22, 2008

Building the eCTD at Regus Victoria

October 27, 2008

Regulatory Affairs Strategies at Regus Victoria

October 28, 2008

Environmental Risk Assessment of Human Pharmaceuticals at Regus Victoria

October 29, 2008

Understanding US-FDA Drug Submission Procedures at Regus Victoria

October 29, 2008

Advanced Pharmacokinetics at Regus Victoria

October 29, 2008

Devising Successful CRO Contracts at Regus Victoria

November 3, 2008

Toxicology at Regus Victoria

November 3, 2008

Biocidal Products Directive at Regus Victoria

November 5, 2008

Signal Detection Strategies at Regus Victoria

November 9, 2008

Clinical Research Project Management at Regus Victoria

November 23, 2008

Regulatory Affairs for Biotechnology at Regus Victoria

November 24, 2008

Regulatory Affairs for Phase I Clinical Trials at Regus Victoria

November 25, 2008

Mastering EU Requirements for Product Labelling & Package Leaflets at Regus Victoria

November 30, 2008

Carrying out Batch Record Review and Product Release at Regus Victoria

November 30, 2008

Introduction to Pharmacogenomics at Regus Victoria

December 1, 2008

Preparing the Chemistry and Pharmacy Section of the EU Registration Dossier at Regus Victoria

December 3, 2008

Lifecycle Management of the eCTD at Regus Victoria

December 7, 2008

The European Chemicals Policy - REACH at Regus Victoria

December 8, 2008

Introduction to Toxicology for the Non-specialist at Regus Victoria

December 10, 2008

Veterinary Clinical Trials at Regus Victoria

December 10, 2008

Conducting Paediatric Clinical trials at Regus Victoria

January 12, 2009

Regulatory Affairs for Veterinary Medicines at Regus Victoria

January 14, 2009

Scientific Advice at Regus Victoria

January 20, 2009

Introduction to Regulatory Affairs for Medical Devices at Regus Victoria

February 4, 2009

Antibody Display, Selection and Engineering at Regus Victoria

February 8, 2009

Introduction to Pharmaceutical Patents at Regus Victoria

March 1, 2009

Stability Testing for Pharmaceutical Products at Regus Victoria

March 10, 2009