M usha rani (42 resultados)

Condición: New. pp. [xii] + 188.

Condición: New. pp. [xii] + 188 Index 1st Published.

Condición: New. pp. [xii] + 188.

Condición: New. pp. 208 Illus.

Condición: New. pp. 208.

Condición: New. pp. 208.

Condición: New. pp. x + 406 Illus.

Condición: New. pp. x + 406.

Condición: New. pp. x + 406.

Hardcover. Condición: New. Brand new book, sourced directly from publisher. Dispatch time is 7-8 days from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

Condición: New.

Condición: New.

Condición: New.

paperback. Condición: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condición: As New. Unread book in perfect condition.

Hardcover. Condición: New. Brand new book, sourced directly from publisher. Dispatch time is 24-48 hours from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

Condición: As New. Unread book in perfect condition.

Condición: New. In English.

Condición: New. pp. 350 1st Edition.

paperback. Condición: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condición: New.

Hardback. Condición: New. 1st. Regulatory bodies such as the European Medicine Agency have done tremendous work in collaboration with experts from the field to develop Good Clinical Practices that apply not only in Europe but also in emerging countries. Designed to be a teaching aid and reference guide, A Practical Guide to Human Research and Clinical focuses on ethics, regulations, and guidelines.Conducting a successful clinical trial requires not only a strong basic knowledge, but also hands-on practical training. The book explains the intricate details of the subject to readers by citing concrete cases, exercises, and templates along with the theoretical aspects. Prof. M.U.R Naidu and his co-authors address all aspects of clinical trials from clinical research, drug development, and quality to methodology, biostatistics, and pharmacovigilance.…

Condición: New. pp. 350.

Condición: New. Naidu, M. U. R. Rani, P. UshaMUR Naidu, Professor and Head, P Usha Rani Additional Professor, Departrnent of Clinical Pharrnacology and Therapeutics, Nizarn s Institute of Medical Sciences, Panjagutta, Hyderabad.Regulatory bodies such as the Eu.

Taschenbuch. Condición: Neu. Study on Effect of Growth Regulators and Micronutrients on Okra growth and yield of Okra | A.esculentus (L.) Moench | Usha Rani M. (u. a.) | Taschenbuch | 100 S. | Englisch | 2013 | LAP LAMBERT Academic Publishing | EAN 9783659212574 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. …

Hardcover. Condición: Brand New. reprint edition. 327 pages. 9.75x6.50x1.00 inches. In Stock.

Hardback. Condición: New. 1st. Regulatory bodies such as the European Medicine Agency have done tremendous work in collaboration with experts from the field to develop Good Clinical Practices that apply not only in Europe but also in emerging countries. Designed to be a teaching aid and reference guide, A Practical Guide to Human Research and Clinical focuses on ethics, regulations, and guidelines.Conducting a successful clinical trial requires not only a strong basic knowledge, but also hands-on practical training. The book explains the intricate details of the subject to readers by citing concrete cases, exercises, and templates along with the theoretical aspects. Prof. M.U.R Naidu and his co-authors address all aspects of clinical trials from clinical research, drug development, and quality to methodology, biostatistics, and pharmacovigilance.…

Contents 1 Clinical Research A Clinical Investigators Perspective 2 Drug and Device Development Process 3 Preclinical Drug Development 4 Phases of Clinical Trials 5 Phase 0 - Microdosing Stdies 6 Clinical Research Planning 7 Clinical Research Design 8 Clinical Research Protocol 9 Designing Case Report Forms 10 Process of Randomization in Clinical Trials 11 Investigational Medicinal Products 12 Multicenter Clinical Trials 13 Good Clinical Research Practice 14 Role and Responsibilities of Sponsor 15 Role and Responsibilities of Principal Investigator 16 Ethical Consideration in Clinical Research Special Reference to Developing Countries 17 Informed Consent in Clinical Research 18 Monitoring in Clinical Trials 19 Quality Assurance in Clinical Research 20 Pharmacovigilance and Drug Safety 21 Data and Safety Monitoring Board and Monitoring Plan 22 Standard Operating Procedures 23 Archiving Clinical Research Documents 24 Evidence Based Medicine 25 Clinical Research Data Management 26 Clinical BiostatisticsAbout the Book Many health professionals are expected to conduct their own trial or to participate in trials by recruiting subjects Everyone who is conducting clinical research should have a sufficient understanding of the scientific and administrative aspect including an awareness of the regulation and guidelines associated with clinical trials This textbook addresses many issues of human clinical research and clinical trials and provides comprehensive overview of the design conduct and analysis of all the phases of clinical trials It is aimed at health and other research professionals and students Salient Features Book can be used as teaching aid and as a reference guide  Important concepts are presented throughout the chapters with diagrams and check lists.…

Condición: New.

Condición: New.