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Fri, Nov 13, 2009 9:00am		Surviving as a Woman in Science - Conference (BioPark Hertfordshire, Welwyn Garden City) With talks such as "Do women make a difference to biology, and does biology make a difference to women?" (Professor Sian Harding, Imperial College, London) and "PhD and Business" (Dr Mitra Hedman, SolXO Ltd, UK) this event will be extremely interesting for women working in science.
Mon, Nov 16, 2009		GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India - Course / Training / Workshop (Taj Lands End, Mumbai, India) The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business.
Mon, Nov 16, 2009 9:00am		Generic Medicine: IP / Legal and Regulatory Issues - Seminar (TAJ Hotels) To be held in 3 Indian cities: Mumbai, Delhi and Hyderabad. The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business. Topics to be covered include:  Understand the European Generic marketplace  Patents and how they affect generics  Data Exclusivity  DCP and European Regulatory System  Key aspects of European legislation
Wed, Nov 18, 2009		GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India - Course / Training / Workshop (Taj Palace, New Delhi, India) The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business.
Wed, Nov 18, 2009 9:00am		Generic Medicine: IP / Legal and Regulatory Issues - Seminar (TAJ Hotels) To be held in 3 Indian cities: Mumbai, Delhi and Hyderabad. The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business. Topics to be covered include:  Understand the European Generic marketplace  Patents and how they affect generics  Data Exclusivity  DCP and European Regulatory System  Key aspects of European legislation
Thu, Nov 19, 2009		European Regulatory Affairs - Course / Training / Workshop (SAS Radisson Hotel Boulogne) This training course will provide an excellent introduction to the European Regulatory Procedures for personnel in regulatory affairs, clinical research, project management and other disciplines involved in the development of medicinal products. The course will cover the evolution of the Registration Systems available for approval of products since January 1995 in the European Union, together with major changes in New Medicines Legislation. Title IV of Regulation EC726/2004 on the European Medicines Agency -Responsibilities and Administrative Structure, came into effect on May 20, 2004. The remainder of the Regulation and all of Directive 2004/27/EC became effective in November 20, 2005. The very important changes in New Medicine Legislation concerning regulatory procedures, access to Centralised and Mutual Recognition Procedures, reduction in Regulatory Data protection will be described in detail. Detailed review will be offered on the changed Centralised and Mutual Recognition Procedures and New Decentralised Procedure with discussion of practical examples of product types suitable for each procedure. Other issues that impact on successful regulatory strategy in Europe, Harmonisation of Summary of Product Characteristics, Article 30 and Article 31 referrals and Supplementary Protection Certificate for Patents will be described. Also reviewed and discussed is the legal status of medicinal products and the procedure for switching from prescription only sale to OTC sale, legislation controlling Medical Devices and the Clinical Trial Directive. The workshop will provide strategic advice on how to file applications for the marketing authorisations in the European Union for staff involved in Regulatory Affairs. Regulatory strategy which impacts on commercial, business and licensing arrangements will be of importance to those responsible for business development.
Fri, Nov 20, 2009		European Regulatory Affairs - Course / Training / Workshop (SAS Radisson Hotel Boulogne) This training course will provide an excellent introduction to the European Regulatory Procedures for personnel in regulatory affairs, clinical research, project management and other disciplines involved in the development of medicinal products. The course will cover the evolution of the Registration Systems available for approval of products since January 1995 in the European Union, together with major changes in New Medicines Legislation. Title IV of Regulation EC726/2004 on the European Medicines Agency -Responsibilities and Administrative Structure, came into effect on May 20, 2004. The remainder of the Regulation and all of Directive 2004/27/EC became effective in November 20, 2005. The very important changes in New Medicine Legislation concerning regulatory procedures, access to Centralised and Mutual Recognition Procedures, reduction in Regulatory Data protection will be described in detail. Detailed review will be offered on the changed Centralised and Mutual Recognition Procedures and New Decentralised Procedure with discussion of practical examples of product types suitable for each procedure. Other issues that impact on successful regulatory strategy in Europe, Harmonisation of Summary of Product Characteristics, Article 30 and Article 31 referrals and Supplementary Protection Certificate for Patents will be described. Also reviewed and discussed is the legal status of medicinal products and the procedure for switching from prescription only sale to OTC sale, legislation controlling Medical Devices and the Clinical Trial Directive. The workshop will provide strategic advice on how to file applications for the marketing authorisations in the European Union for staff involved in Regulatory Affairs. Regulatory strategy which impacts on commercial, business and licensing arrangements will be of importance to those responsible for business development.
Fri, Nov 20, 2009		GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India - Course / Training / Workshop (Taj Krishna, Hyderabad, India) The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business.
Fri, Nov 20, 2009 9:00am		Generic Medicine: IP / Legal and Regulatory Issues - Seminar (TAJ Hotels) To be held in 3 Indian cities: Mumbai, Delhi and Hyderabad. The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business. Topics to be covered include:  Understand the European Generic marketplace  Patents and how they affect generics  Data Exclusivity  DCP and European Regulatory System  Key aspects of European legislation
Wed, Dec 2, 2009		Pharma partnering event PharmaVenue - Conference (AB Skipper Hotel Barcelona (Spain)) PharmaVenue offers an unparalleled opportunity to identify new business opportunities and meet decision makers to forge new partnerships in the field of * Innovations, * Generics and * OTC/Healthcare products PharmaVenue can help your business get to the next level through quality one-to-one meetings with senior level executives. Our state-of-the art interactive partnering software enables you to efficiently select the most attractive license opportunities, pre-arrange and conduct many productive business meetings to unlock future revenue streams. * By having access to detailed information on key license projects of each participating company prior to the event and with help of several new interactive networking tools we facilitate the process of screening potential opportunities and partners. * During six weeks, you may easily submit and review meeting requests through the password protected web-site. You will have access to your individual meeting schedule one week prior to the event and may make your final adjustments to your agenda. Our sophisticated software pre-schedules more than 95%* of all meeting requests. * Experience more productive business meetings in two days than in the entire rest of the year.
Thu, Dec 3, 2009		Pharma partnering event PharmaVenue - Conference (AB Skipper Hotel Barcelona (Spain)) PharmaVenue offers an unparalleled opportunity to identify new business opportunities and meet decision makers to forge new partnerships in the field of * Innovations, * Generics and * OTC/Healthcare products PharmaVenue can help your business get to the next level through quality one-to-one meetings with senior level executives. Our state-of-the art interactive partnering software enables you to efficiently select the most attractive license opportunities, pre-arrange and conduct many productive business meetings to unlock future revenue streams. * By having access to detailed information on key license projects of each participating company prior to the event and with help of several new interactive networking tools we facilitate the process of screening potential opportunities and partners. * During six weeks, you may easily submit and review meeting requests through the password protected web-site. You will have access to your individual meeting schedule one week prior to the event and may make your final adjustments to your agenda. Our sophisticated software pre-schedules more than 95%* of all meeting requests. * Experience more productive business meetings in two days than in the entire rest of the year.
Tue, Jan 12, 2010 9:00pm		Biotech Showcase 2010 - Conference Biotech Showcase is a forum devoted to providing biotechnology companies, investors and pharmaceutical executives with an opportunity to meet in one place during the course of one of the largest annual healthcare investor conference that attracts investors and biopharmaceutical executives from around the world. Now in its second year, the event will expand to a second day and include public biotech companies. The two-day program will feature multiple tracks of presenting companies, plenary sessions, an opportunity to schedule one-to-one partnering meetings and networking. The attendees for the showcase will include private and public equity investors, analysts, bankers, biopharmaceutical industry executives and other industry professionals. The Biotech Showcase is produced by Demy-Colton Life Science Advisors and EBD Group. Both organizations have a long history of providing high quality business support services to the biotechnology industry.
Wed, Jan 13, 2010 9:00pm		Biotech Showcase 2010 - Conference Biotech Showcase is a forum devoted to providing biotechnology companies, investors and pharmaceutical executives with an opportunity to meet in one place during the course of one of the largest annual healthcare investor conference that attracts investors and biopharmaceutical executives from around the world. Now in its second year, the event will expand to a second day and include public biotech companies. The two-day program will feature multiple tracks of presenting companies, plenary sessions, an opportunity to schedule one-to-one partnering meetings and networking. The attendees for the showcase will include private and public equity investors, analysts, bankers, biopharmaceutical industry executives and other industry professionals. The Biotech Showcase is produced by Demy-Colton Life Science Advisors and EBD Group. Both organizations have a long history of providing high quality business support services to the biotechnology industry.
Tue, Jan 26, 2010 8:55am		World Drug Delivery and Formulation 2010 - Conference (Radisson BLU Scandinavia Hotel, Dusseldorf, Germany) 26-27th January 2010 Radisson BLU Scandinavia Hotel, Dusseldorf, Germany With increasing generic competition, challenging molecules coming through discovery and continual pressure to produce cost-effective drugs, companies are increasingly turning to formulation and delivery to secure the success of current and new drug products. World Drug Delivery and Formulation 2010 is the event this year for both scientific and business leaders working in formulation and delivery to debate the challenges affecting them. This multi stream delivery and formulation event will focus on both scientific and business issues. This will give everyone the perfect opportunity to attend sessions dedicated to their main area of interest, whilst networking with scientific and business peers from across the entire formulation and delivery spectrum.
Wed, Jan 27, 2010 8:55am		World Drug Delivery and Formulation 2010 - Conference (Radisson BLU Scandinavia Hotel, Dusseldorf, Germany) 26-27th January 2010 Radisson BLU Scandinavia Hotel, Dusseldorf, Germany With increasing generic competition, challenging molecules coming through discovery and continual pressure to produce cost-effective drugs, companies are increasingly turning to formulation and delivery to secure the success of current and new drug products. World Drug Delivery and Formulation 2010 is the event this year for both scientific and business leaders working in formulation and delivery to debate the challenges affecting them. This multi stream delivery and formulation event will focus on both scientific and business issues. This will give everyone the perfect opportunity to attend sessions dedicated to their main area of interest, whilst networking with scientific and business peers from across the entire formulation and delivery spectrum.
Thu, Jul 1, 2010		EU PHARMACEUTICAL REGULATIONS ~ For the Pharmaceutical and Biotechnology Industries - An up-to-date Overview of Current EU Requirements - Course / Training / Workshop (Hotel to be Advised, London, UK) Regulatory Affairs has an acknowledged important role in the pharmaceutical industry, both in obtaining and maintaining marketing authorisations, therefore, knowledge of the current European requirements and the impact of legislative changes on the businesses are essential. This two-day seminar will: Explain how to obtain and maintain marketing authorisations, Provide an up-to-date overview of current EU regulatory requirements and procedures, Offer interactive presentations, Include two workshops designed to look at the practical implementation, Consolidate the information presented during the two days.
Fri, Jul 2, 2010		EU PHARMACEUTICAL REGULATIONS ~ For the Pharmaceutical and Biotechnology Industries - An up-to-date Overview of Current EU Requirements - Course / Training / Workshop (Hotel to be Advised, London, UK) Regulatory Affairs has an acknowledged important role in the pharmaceutical industry, both in obtaining and maintaining marketing authorisations, therefore, knowledge of the current European requirements and the impact of legislative changes on the businesses are essential. This two-day seminar will: Explain how to obtain and maintain marketing authorisations, Provide an up-to-date overview of current EU regulatory requirements and procedures, Offer interactive presentations, Include two workshops designed to look at the practical implementation, Consolidate the information presented during the two days.

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