Taking advantage of liberal regulations under the current world trade
regime that permit the separation of manufacturing from marketing, many
pharmaceutical companies (like other companies) outsource the actual
manufacture of their products. However, because the quality of medicines is
crucial to public health, the pharmaceutical industry is perhaps the most
regulated of all industries. In most countries medicines are controlled prior
to their marketing, and their manufacture is carried out under strict
supervision. Necessarily, numerous international initiatives have led to
elaboration of standards relating to the manufacture and marketing of
medicines. These standards impose stringent rules on all parties to
pharmaceutical manufacturing contracts.
This very useful book provides a comprehensive global guide to the legal
issues and procedures involved in outsourcing the manufacture of medicines. It
describes the legal requirements relating to the manufacture and distribution
of medicines, emphasising the impact of regulatory supervision on the rights
and obligations of persons who outsource manufacturing of medicines and on
those who provide the manufacturing services. The author provides detailed
coverage of such pertinent topics as the following:
• definition of ‘medicine’ in different jurisdictions;
• categories of medicines;
• manufacturing and importation regulation in numerous jurisdictions
worldwide;
• inspection regimes;
• good manufacturing practice (GMP);
• marketing authorization;
• manufacturing documentation;
• complaints and product recall;
• liability insurance;
• protection of trade secrets;
• data exclusivity and data protection;
• deficiencies and delays; and
• recognition and enforcement of judgements.
A significant part of the book is devoted to cross-border problems arising
from such matters as conflict of laws or taxation.
Indispensable to counsel for pharmaceutical companies of any size, Contract
Manufacturing of Medicines will also be of great value to practitioners
and academics concerned with international trade for its precise, in-depth
delineation of the inner workings of a complex and highly significant trade
regime.
Preface,
Chapter 1 Outsourcing of
Manufacturing in the Pharmaceutical Industry Chapter 2 Basic
Definitions Chapter 3 Manufacturing and Importation of Medicines –
Legal Aspects Chapter 4 The Good Manufacturing Practice Chapter 5
Contract Manufacturing – Basic Requirements Chapter 6 Regulatory
Affairs Chapter 7 Quality Assurance – Basic Requirements
Chapter 8 The Role of the Authorized/Qualified Person Chapter 9
Liability for Defective Products Chapter 10 Confidentiality Chapter
11 Intellectual Property Chapter 12 Deliveries – Terms and
Conditions Chapter 13 Disputes between the Parties Chapter 14
Taxes, Duties and Additional costs Chapter 15 Manufacturing of API
Chapter 16 Conclusions
Appendix,
Bibliography, Index