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PHARMACEUTICAL PRODUCT LICENSING

Không đóng trình duyệt đến khi xuất hiện nút TẢI XUỐNG

Any book written about a subject which is rapidly changing necessarily represents a ‘snapshot’ in time—the author’s attempts to describe the current situation, and to predict what might be the state of things when the book is published. In the case of this book, the speed of change is rapidly increasing as the European Community (EC) nears 31 December 1992, the target date which the Single European Act defines as that by which a Single Market in products should be established.

TÀI LIỆU LIÊN QUAN

Using NMR, X-ray, and CD analysis in the study on natural products obtained from Vietnamese plant and fungi in terms of pharmaceutical product development

A perspective of risk assessment for product developments in biotechnology and pharmaceutical products

Environmental Toxicology Third Edition

Developing a process of preparing fallopia multiflora thunb. and proposing basic standards for the product

Pharmaceutical crystallization in CouetteTaylor crystallizer: A case study of polymorphism of amino acid L-glutamic acid

TYING ODYSSEUS TO THE MAST: EVIDENCE FROM A COMMITMENT SAVINGS PRODUCT IN THE PHILIPPINES*

Information as a product: not goods, not services

PHARMACEUTICAL PRODUCT LICENSING
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