Kashmir

https://www.cliniindia.com

LEARN CLINICAL RESEARCH ONLINE LIVE LECTURES WITH LMS ACCESS
ISO 9001: 2015 | SAS Accredited Institute
Technology-driven Research and Innovative (TRIP) Pedagogy

At the Clini India, we are dedicated to providing comprehensive and cutting-edge training programs to individuals seeking a successful career in the pharmaceutical, life science, and medical fields. Our institute specializes in Clinical Research, Clinical Data Management, Pharmacovigilance, and Medical Writing domains, ensuring that our graduates are well-equipped with the knowledge and skills needed to work in these dynamic industries.

Program Offered- Advance Program in Clinical Research & Management (APCRM)

Duration: 4 Months
Mode: Live Lectures along with LMS Access
Pre-Recruitment Training with Placement Support

Modules Covered

• Clinical Trial Operations
• Clinical Data Management
• Pharmacovigilance
• Medical Writing
• Soft Skills/ Communication Skills Classes

WHO CAN JOIN
B.Pharm/ M.Pharm/ Pharm.D
B.Sc/ M.Sc/ Phd Life Sciences/ Chemistry
MBBS/ BDS/ BAMS/ BHMS etc.
BPT/ MPT etc.

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WHY CLINI INDIA

LIVE Online Training with Virtual Classroom

• A SAS Accredited Clinical Research Institute
• ISO 9001: 2015 Clinical Research Institute
• Learning Management System Access (LMS) (24X7) - With Video, Presentations, e-books and Podcasts.
• Placement Support- with direct team access.
• India's most trusted clinical research training institute for Industry oriented training.

Why Choose Us?

Be a part of Technology-driven Research and Innovative (TRIP) Pedagogy

• SAS Accreditation: Clini India proudly holds SAS Accreditation, a testament to our commitment to delivering high-quality education. As a student, this accreditation adds value to your resume and validates the proficiency you will gain through our program.
• Expert Faculty: Our experienced faculty members possess extensive industry knowledge and expertise. They are passionate about sharing their insights and ensuring that our students receive top-notch education and guidance.
• Industry-Relevant Curriculum: Our carefully crafted curriculum is designed in collaboration with industry professionals, keeping pace with the latest advancements and trends in the field of clinical research. We provide our students with practical, real-world scenarios and case studies to enhance their learning experience.
• Hands-On Training: We strongly believe in the importance of practical training. Our state-of-the-art training facility offers hands-on training sessions, allowing students to apply their theoretical knowledge in a simulated clinical research environment.
• Comprehensive Programs: We offer a range of comprehensive training programs that cover all essential aspects of Clinical Research, Clinical Data Management, Pharmacovigilance, and Medical Writing. Our programs cater to individuals with varying levels of experience, from beginners to seasoned professionals looking to enhance their skills.

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APCRM Program Offerings:

• Clinical Research Training: Our Clinical Research Training program equips students with a deep understanding of clinical trials, regulatory requirements, good clinical practices (GCP), and ethical considerations. Students will gain hands-on experience in protocol development, study design, data collection, and analysis.
• Clinical Data Management: In our Clinical Data Management program, students learn the fundamentals of data management processes, data validation, database design, and quality control. They will also become proficient in using industry-standard tools and technologies for data capture and analysis.
• Pharmacovigilance Training: Pharmacovigilance is a critical aspect of drug safety and surveillance. Our Pharmacovigilance Training program covers adverse event reporting, signal detection, risk assessment, and regulatory compliance. Students will gain practical experience in managing safety databases and ensuring compliance with global pharmacovigilance guidelines.
• Medical Writing: Our Medical Writing program focuses on developing the necessary skills to produce high-quality clinical research documents, such as clinical study reports, protocols, regulatory submissions, and scientific manuscripts. Students will learn about effective writing techniques, document structure, and adherence to industry guidelines.

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Career Opportunities:

Upon completion of our training programs, graduates can explore a wide range of career opportunities, including:

• Clinical Research Coordinator (CRC)
• Clinical Research Associate (CRA)
• Clinical Data Manager
• Pharmacovigilance Specialist
• Medical Writer
• Regulatory Affairs Associate
• Clinical Project Manager
• Drug Safety Associate
• Quality Assurance Specialist

HOW TO JOIN
Click on the below link below and send your details, we will help you with the Program details and registration process.
 
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Visit website- www.cliniindia.com

Pharma Ascent 2023 was held on 2nd April, 2023. Students from different colleges and universities were participated in pre GPAT Exam.

“The International Institute of Health Management Research (IIHMR Delhi), definitely beats the well-renowned B-Schools when it comes to talent placement in the healthcare industry.

The Ministry of Human Resource Development , which is now known as Ministry of Education, Government of India has established the National Testing Agency as an independent, autonomous, and self-sustained premier testing organization under the Societies Registration Act for conducting efficient, transparent and international standards tests in order to assess the competency of candidates for admissions to premier higher education institutions.

Interview of Dr. Montu Patel, President of Pharmacy Council of India (PCI) was conducted on 3rd May 2022 at Ahmedabad, Gujarat.

As the market leader in clinical research analytics, SAS provides a secure analytics foundation and scalable framework for clinical analysis and submission.

SAS is the de facto standard for clinical trials, data analysis and reporting for new product submissions to regulatory authorities, such as the US Federal Drug Administration.
SAS is widely recognized as the gold standard for determining safety and efficacy for clinical trials.

The Ministry of Human Resource Development , which is now known as Ministry of Education, Government of India has established the National Testing Agency as an independent, autonomous, and self-sustained premier testing organization under the Societies Registration Act for conducting efficient, transparent and international standards tests in order to assess the competency of candidates for admissions to premier higher education institutions.