Dr neeru agarwal (22 resultados)

PAP. Condición: New. New Book. Shipped from UK. Established seller since 2000.

PAP. Condición: New. New Book. Shipped from UK. Established seller since 2000.

Condición: New. Print on Demand.

Condición: New. Print on Demand.

Condición: New. Print on Demand.

Paperback / softback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Paperback / softback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Paperback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Condición: New. Print on Demand.

Condición: New. Print on Demand.

Condición: New. Print on Demand.

Paperback. Condición: new. Paperback. Question Booklet, Volume 1 - An extensive collection of puzzles such as crosswords, Word search, Match the following, Full Forms, Identify the medical sign etc. which helps Pre-Med, Medical, and Nursing Students, EMTs, Massage Therapists and Other Health Care Professionals and Crossword Lovers to test their medical knowledge while pursuing any nursing and pharmacology course. It is a supplemental study and review tool in a different puzzle formats using terminology of anatomy, physiology, pathology, and all sciences concerned with the human body. The unique feature of this book is that it includes some basic medical sign language which teaches medical students how to understand the special patients who cannot speak. It is a compilation of medical terminology and its related field which is designed for students of medicine and related health sciences and practitioners of these fields of study. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Condición: New. Print on Demand.

Paperback / softback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Paperback / softback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Paperback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Paperback / softback. Condición: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Paperback. Condición: new. Paperback. Clinical trials are the mainstay for bringing out new drugs to the market and constitute approximately 70% of the total time and money spent in drug development. Typically it takes approximately 12 years and US$ 1 billion to bring one new drug from conception to market out of which 6 to 7 years are usually spent in various phases of clinical trials. In order to develop a comprehensive understanding on clinical research, it is important to understand the overall drug discovery process.This comprehensive and well-organized text is grounded in real-world applications of theoretical concepts of Drug discovery and development. It properly explains how many and what clinical trials are conducted to bring any medicine in the market for human consumption. It highlights the regulatory environment of India w.r.t to Clinical research, trials, and drug development. A very easy way to understand what are the roles and responsibilities of various clinical trial stakeholders. Basically, its a step by step guide for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, government and legal professions. The text provides exemplary coverage of all the relevant issues. The definitive book on the subject. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Paperback. Condición: new. Paperback. Pharmacovigilance Insight & Global Perspective is a step by step guide for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, government and legal professions. It discussed about evolution of pharmacovigilance, ICH guidelines, Partners in Pharmacovigilance, Regulatory and Legal Aspects, Reporting Requirement and Reporting Forms, Public Safety Update Report, Individual Case Safety Report, Signal Detection, PV Inspections, Expedited Reporting Requirements, Global Perspective of Pharmacovigilance and Adverse Drug Reaction (ADR) Reporting, List of Technical Assistance providers in Pharmacovigilance, MedDRA, PV Glossary etc. The text provides exemplary coverage of all the relevant issues. The definitive book on the subject. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Paperback. Condición: new. Paperback. Advanced View on Pharmacology Glossary and abbreviation provides a convenient personal reference source, intended to complement more encyclopaedic works. First, there is an alphabetic, fully cross-indexed listing of pharmacologically terms. Emphasis in explanation is given to terms that can cause confusion, for example those relating to drug receptors and to endogenous mediators Secondly, it also gives readers a basic understanding of the basics of Pharmacology, fundamentals of Pharmacodyanamics and Pharmackinetics and various processes involved. Audience: This work provides indispensable information for researchers in the fields of pharmacology, medicinal chemistry and pharmaceutics, and biochemistry, as well as for medical and science writers and editors and drug regulatory officers This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Paperback. Condición: new. Paperback. This comprehensive and well-organized text is grounded in real-world applications of theoretical concepts of Drug discovery and development. It properly explains how many and what clinical trials are conducted to bring any medicine in the market for human consumption. It highlights the regulatory environment of India w.r.t to Clinical research, trials, and drug development. A very easy way to understand what are the roles and responsibilities of various clinical trial stakeholders. Basically, its a step by step guide for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, government and legal professions. The text provides exemplary coverage of all the relevant issues. The definitive book on the subject This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Paperback. Condición: new. Paperback. This comprehensive and well-organized text is grounded in real-world applications of theoretical concepts of Clinical Research with a primary focus on Drug development and clinical trial processes, Good Clinical Practices (GCP) guidelines, Drug regulatory affairs, Roles and responsibilities of various clinical trial stakeholders etc. A step by step guide for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, government and legal professions. The text provides exemplary coverage of all the relevant issues. The definitive book on the subject This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…