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Related Events

Future Events

Introduction to Regulatory Affairs for Biotech

Introduction to Regulatory Affairs for Biotech

Dates: 22 May 2012 - 24 May 2012
Venue: MWB Victoria

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

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

Dates: 22 May 2012 - 24 May 2012
Venue: Green Park Hilton

Conducting Paediatric Clinical Trials

Conducting Paediatric Clinical Trials

Dates: 13 Jun 2012 - 14 Jun 2012
Venue: MWB Victoria

Gaining Marketing Authorisations in CIS

Dates: 13 Jun 2012 - 14 Jun 2012
Venue: MWB Victoria

Introduction to European Regulatory Affairs

Dates: 19 Jun 2012 - 21 Jun 2012
Venue: Regus Princeton - Forrestal Village, New Jersey, USA

Advanced European Regulatory Affairs

Advanced European Regulatory Affairs

Dates: 26 Jun 2012 - 28 Jun 2012
Venue: MWB Victoria

European Regulatory Affairs School

European Regulatory Affairs School

Dates: 27 Jun 2012 - 29 Jun 2012
Venue: London

Intermediate Level Adverse Event Reporting

Intermediate Level Adverse Event Reporting

Dates: 04 Jul 2012 - 05 Jul 2012
Venue: MWB Edinburgh

Dissolution Testing

Dissolution Testing

Dates: 10 Jul 2012 - 11 Jul 2012
Venue: NH Amsterdam Centre

Regulatory Affairs for Biotech

Dates: 17 Jul 2012 - 18 Jul 2012
Venue: Regus Boston Independence Wharf, Boston, USA

Filing Variations

Filing Variations

Dates: 19 Jul 2012 - 20 Jul 2012
Venue: Kempinski Hotel Bristol, Berlin

Adverse Event Reporting & Pharmacovigilance

Adverse Event Reporting & Pharmacovigilance

Dates: 24 Jul 2012 - 25 Jul 2012
Venue: Hotel le Plaza, Brussels, Belgium

Introduction to European Regulatory Affairs

Introduction to European Regulatory Affairs

Dates: 21 Aug 2012 - 23 Aug 2012
Venue: MWB Cambridge

Scientific Advice

Dates: 06 Sep 2012 - 07 Sep 2012
Venue: MWB Edinburgh

US-FDA Drug Submission Procedures

US-FDA Drug Submission Procedures

Dates: 11 Sep 2012 - 12 Sep 2012
Venue: MWB Victoria

Adverse Event Reporting & Pharmacovigilance

Adverse Event Reporting & Pharmacovigilance

Dates: 13 Sep 2012 - 14 Sep 2012
Venue: MWB Victoria

Regulatory Affairs Strategies

Regulatory Affairs Strategies

Dates: 20 Sep 2012 - 21 Sep 2012
Venue: MWB Victoria

Registration of Pharmaceuticals in the EU

Registration of Pharmaceuticals in the EU

Dates: 09 Oct 2012 - 11 Oct 2012
Venue: MWB Victoria

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

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

Dates: 16 Oct 2012 - 18 Oct 2012
Venue: Hotel le Plaza, Brussels, Belgium

Introduction to European Regulatory Affairs

Dates: 17 Oct 2012 - 19 Oct 2012
Venue: REGUS Boston Prudential Tower, Boston, USA

Gaining Marketing Authorisations in CIS

Dates: 17 Oct 2012 - 18 Oct 2012
Venue: Renaissance Polat Istanbul Hotel

Regulatory Affairs for Preclinical Safety Studies

Regulatory Affairs for Preclinical Safety Studies

Dates: 18 Oct 2012 - 19 Oct 2012
Venue: MWB Victoria

Advanced European Regulatory Affairs

Advanced European Regulatory Affairs

Dates: 23 Oct 2012 - 25 Oct 2012
Venue: MWB Victoria

Dissolution Testing

Dissolution Testing

Dates: 06 Nov 2012 - 07 Nov 2012
Venue: MWB Victoria

Mastering EU Requirements for Product Labelling and Package Leaflets

Mastering EU Requirements for Product Labelling and Package Leaflets

Dates: 06 Nov 2012 - 08 Nov 2012
Venue: MWB Victoria

Filing Variations

Filing Variations

Dates: 15 Nov 2012 - 16 Nov 2012
Venue: MWB Victoria

Regulatory Affairs for Biotech

Dates: 27 Nov 2012 - 28 Nov 2012
Venue: Regus Mission Valley, San Diego, California, USA

Adverse Event Reporting & Pharmacovigilance

Adverse Event Reporting & Pharmacovigilance

Dates: 04 Dec 2012 - 05 Dec 2012
Venue: MWB Victoria

Intermediate Level Adverse Event Reporting

Intermediate Level Adverse Event Reporting

Dates: 06 Dec 2012 - 07 Dec 2012
Venue: MWB Victoria

Conducting Paediatric Clinical Trials

Conducting Paediatric Clinical Trials

Dates: 13 Dec 2012 - 14 Dec 2012
Venue: MWB Victoria

A Practical Guide to Pharmacovigilance and Drug Safety

A Practical Guide to Pharmacovigilance and Drug Safety

Dates: ongoing self study course
Venue: self study course

Pharmaceutical Regulatory Affairs in the EU and US

Pharmaceutical Regulatory Affairs in the EU and US

Dates: Ongoing self study course
Venue: self study course

Patent Law and Practice in Pharmaceuticals

Patent Law and Practice in Pharmaceuticals

Dates: 10 Week self study course
Venue: self study course


Past Events

Signal Detection Strategies

Signal Detection Strategies

Dates: 08 Nov 2011 - 09 Nov 2011
Venue: MWB Victoria

Introduction to European Regulatory Affairs

Introduction to European Regulatory Affairs

Dates: 17 Apr 2012 - 19 Apr 2012
Venue: Renaissance Zurich Hotel



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Dates and Venues

22 May 2012 - 23 May 2012

MWB Victoria

19 Sep 2012 - 20 Sep 2012

MWB Victoria

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