Anderson | Drafting Agreements in the Biotechnology and Pharmaceutical Industries | Loseblattwerk | sack.de

Loseblattwerk, Englisch, Format (B × H): 171 mm x 246 mm

Anderson

Drafting Agreements in the Biotechnology and Pharmaceutical Industries

Loseblattwerk, Englisch, Format (B × H): 171 mm x 246 mm

ISBN: 978-0-19-953963-5
Verlag: Oxford University Press


This looseleaf provides precedent agreements and legal commentary in relation to the main types of commercial transaction encountered in the life-cycle of a product in the biotechnology and pharmaceutical industries. Each agreement is accompanied by detailed commentary on legal, commercial and practice issues. In addition the commentary highlights important differences between English law and other key EU jurisdictions comprising Germany, France, the Netherlands, Spain and Sweden
with specific commentary being provided by specialist lawyers within these countries. Further commentary on the US specific issues is provided in the first updating release.

The third part of the looseleaf incorporates a separate summary and discussion of legal issues that are common to different types of agreement, relevant statutory and legal materials and website links to other relevant materials.

The looseleaf is published with an accompanying online resource providing plain versions of all the precedents which can be downloaded and edited to enable the user to create and amend precedents based on those provided by the work.
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Zielgruppe


Lawyers and commercial managers who are involved in drafting and negotiating agreements in the biotechnology and pharmaceutical industries, including university technology transfer managers, IP licensing practitioners and product development managers in biotechnology or pharmaceutical companies.

Weitere Infos & Material


Part A: Introduction
1: Introduction to agreements in the Bio/Pharma sector
Part B: Annotated precedents
2: Preliminary agreements
3: Collaborative research and development agreements
4: Services agreements
5: Clinical trials agreements
6: Product manufacturing and supply agreements
7: Distribution and marketing agreements
8: Licence agreements
9: Assignments
Part C: General commentary
10: Regulations affecting the research and development of pharmaceutical products
11: Intellectual property law in Europe
12: Competition law issues
13: Contract law and practice
14: Tax and currency issues
Part D: Materials
16: Selected EC competition law materials
17: Web-site links to other selected materials


Mark is a solicitor and former barrister, recognised as a leading adviser in the field of life sciences transactions. He has a degree in law from Durham University. Mark founded Anderson & Company in 1994.

Caroline de Mareuil-Villette is a European Patent Attorney at Cabinet Plasseraud, France

Magali Touroude is a European Patent Attorney at Cabinet Plasseraud, France

Dr Christine Kanz is a Partner and Attorney at Reimann Osterrieth Köhler Haft, Germany

Dr Heike Wachenhausen is a Lawyer at Anwaltskanzlei Sträter, Germany

Carla Schoonderbeek is a Partner and Head of the Life Sciences team at Nauta Dutilh, Netherlands

Eric Runesson is a Partner at Sandart & Partners, Sweden

Pablo Olivera is a Partner at Garrigues, Spain

Dulce Mª Miranda Naranjo is a European Patent Attorney, Garrigues, Spain

Gina M. Bicknell is an associate with Marshall, Gerstein & Borun, USA

Pamela L. Cox is a partner at Marshall, Gerstein & Borun, USA

Patrick D. Ertel is a partner at Marshall, Gerstein & Borun, USA


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