الأبحاث السريرية
Пример тестовых заданий для оформления сертификата GCP в 2020-2021 году 1) При использовании перекресного дизайна при исследованиях биоэквивалентности: أ) пациентам группы назначается одинаковое лечение. ب) пациенты, при помощи процедуры рандомизации, распределяются на قراءة المزيد…
A Clinical Research Associate (CRA) is a profession defined by Good clinical practice guidelines (I GCP). The main function of a clinical research associate is to monitor clinical trials. He or she may work directly with the sponsor قراءة المزيد…
NBScience ___________________________ providing smart solutions for clinical research industries NBScience – an independent private company offering to Clients wide range of services in the area of clinical research industry. NBScience is a full service local قراءة المزيد…
Planned List of NBScience medical seminars in Kazakhstan , Belorussia , روسيا -2018 – 2021 1) April 14-15, 2021 ” ممارسة سريرية جيدة” 2) مايو 23-24,2021 ” ممارسات التصنيع الجيدة” 3) June 02-03,2021″الأبحاث السريرية” 4) قراءة المزيد…
Stem Cell – 2018 اكتوبر 21-22, 2018 medical conference Title: Stem cell-2018 Location: كييف,Ukraine Venue: Speakers: Dr Eugene Zadorin Dr Andrew Gilbert ( Canada) Topics: Cell Therapy & Regenerative Medicine Cancer stem cells as قراءة المزيد…
العلاج بالخلايا الجذعية – 2019 international medical conference 01-02 اكتوبر, 2019 Vravrona Attica – Greece (deadline for registration – يونيو 27, 2018) Programme: يوم 1 (اكتوبر 01,2019) 9.00 – 9.15 Welcome and Introduction 9.15-10.00 Spinal Cord قراءة المزيد…
Artificial embryonic stem cells tested in people for first time By the first time, a new type of stem cell, derived from “virgin births”, has been tested in people. The cells have been injected into قراءة المزيد…
عنوان: Actual issues of Ophthalmology Location: أوكرانيا الوصف: Actual issues of Ophthalmology Start Date: 2018-09-29 تاريخ الانتهاء: 2018-09-30
Responsibilities The Director, GCP will be required to oversee all and participate in, quality assurance auditing of all activities subject to the, “ICH Good Clinical/Laboratory Practice: Consolidated Guideline,” (GCP/GLP’s), supporting a program of quality assurance قراءة المزيد…
Responsibilities Assisting in the design and execution of high quality clinical studies in compliance with FDA and ICH requirements. Function as a primary liaison to clinical investigators/site staff. Identify, qualify, initiate, monitor and close out قراءة المزيد…
List of medical conferences in Ukraine – 2018 Musculoskeletal Diseases 10-11 March Lviv Emergency conditions and disaster medicine March 31 – April 1 Kiev Recent advances in the prevention and treatment قراءة المزيد…
Responsibilities Duties: The Clinical Research Administrator reviews applications for research projects to ensure that protocols meet regulatory and ethical standards for the protection of human or animal subjects. Requirements Minimum Requirements: This position requires a قراءة المزيد…
ممارسة سريرية جيدة
مدقق حسابات, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, “ICH Good Clinical Practice: Consolidated Guideline,” (GCPs), supporting a program of quality assurance (QA) to ensure that قراءة المزيد…
Responsibilities As part of this dynamic Cancer Center CTO team, Clinical Research Coordinators will manage & oversee several oncology clinical trials, from study inception to termination. Responsibilities for this position include but are not limited قراءة المزيد…
Contract research organisations (CROs) by Peter Hogg ProClinical Life Sciences have become essential to the pharma, biotech, and medtech industries by supporting clients’ efforts to test, refine, and market the latest pharmaceuticals and medical قراءة المزيد…
