Cliniminds India
Cliniminds was established in Year 2004 – Tenet Health Edutech Pvt. Ltd., promoted by team of Industry professionals and academia. Its India’s first skill development institution in life sciences domain to receive Pharmaceutical Society of India (PSI), Accreditation Council for Clinical Research Education (ACCRE U.S.).
Following courses we offer; Advanced Post Graduate Diploma in Pharmacovigilance, Data Management & SAS, Advanced Post Graduate Diploma in Pharmacovigilance & Medical Writing, Post Graduate Diploma in Medical & Scientific Content Writing, Advanced Post Graduate Diploma in Pharmacovigilance.
We offer wide range of skill development clinical research, pharmaceutical and healthcare educational programs and training solutions
Our programs sustained by superior copyright content and faculty with global stand point.
We have national Presence – 15 major cities in India, International Centers: USA ; UK, RUSSIA and UAE
For more information contact : [email protected]
Мастер-файл системы фармаконадзора
Cliniminds – Исследования биодоступности и биоэквивалентности
Уполномоченное лицо по фармаконадзору (QPPV)
Уполномоченное лицо по фармаконадзору (QPPV)
Стандартные операционные процедуры и процедурные документы - Аудиты и инспекции по фармаконадзору
Рабочий процесс PV - Аудиты и инспекции фармаконадзора
Ориентация Cliniminds: вопросы регулирования лекарственных средств, права интеллектуальной собств...
Подготовка и подача досье Cliniminds: Отдел регулирования лекарственных средств
Career Opportunities in Drug Regulatory Affairs & IPR
CLINIMINDS CASE REPORT FORMS - CLINICAL RESEARCH
Protocol Design - Clinical Research
CTD (Common Technical Document ) Module 1
Cliniminds Literature search - Pharmacovigilance
Aggregate Report Writing Program - PSUR Writing (Periodic Safety Update Reports)
Cliniminds Orientation August 2025 - Drug Regulatory Affairs, IPR & Patents
Cliniminds Orientation July 2025 - Clinical Research, Pharmacovigilance, Clinical Data Management
International Council for Harmonisation (ICH)
Pharmacovigilance Programme of India (PvPI)
Common Technical Documents - Drug Regulatory Affairs
Naranjo Scale - Pharmacovigilance
Data Management Plan (DMP) - Clinical Data Management
Database Lock Point - Clinical Data Management
Principal of ALCOA+ in Clinical Data Management
When did the formal celebration of Clinical Trials Day begin?
User Acceptant Testing - Clinical Data Management
Clinical Trial Agreement (CTA) - Clinical Research
Introduction of PBRER (Periodic Benefit-Risk Evaluation Report) - Aggregate Report Writing
Introduction of Aggregate Report
eCRF Completion Guidelines
New Beginnings, Bright Futures: Celebrating Devesh Aggarwal’s Success