• PG diploma in clinical research & Management.
• PG diploma in Clinical datamanagement
• PG diploma in Pharmacovigilance
• Diploma in Medical coding

Indian Institute of clinical research & Management ((IICRM)) also offers the following course courses looking at current demand in the market.

Why we offer this training?

• Indian pharmaceutical industry is one of the fastest growing sectors of the Indian economy and has made rapid strides over the years. From being import dependent in the 1950s, the industry has achieved self-sufficiency and gained global recognition as a producer of low cost, high quality bulk drugs and formulations. Having proved itself in the international market, India is ready to face the challenges of proving its efficiency as the preferred destination for global clinical trials.
  
  A number of factors favour India as a clinical research hub. Firstly, there are numerous government-funded medical and pharmaceutical institutions with state-of-the-art facilities, which can serve as ideal centers for multi-centered clinical trials. Secondly, India boasts of well-trained and qualified manpower, well versed in English. More importantly, there is vast clinical material, which can be utilized
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  In terms of the cost efficiency, India is a better bet as the cost to conduct a trial here is lower by 50 to 75 percent than in United States or European Union. R&D costs in India are substantially less than those in the developed world and it is possible to conduct both new drug discovery research and novel drug delivery system programs  at competitive rates. In addition, while clinical trials cost approximately $300 to $350 million abroad, they cost about Rs 100 crore in India. There is a good communication link, which favours fast recruitments and approvals. Thus, studies can be completed quickly, providing an edge over competitors.
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Job Prospects
Over the year 25,00000 jobs are available.

About the Placement : IICRM has its proven track record of placement. The placement cell of IICRM proven that no one in the industry can defeat them in placement support.
PG diploma in clinical research & Management.

• PG diploma in Clinical datamanagement
• PG diploma in Pharmacovigilance

These  programs are designed for the professional who wants to transition into a CRA position or enter the clinical research industry. It offers a comprehensive Education and “Hands-On” Training of the clinical research process, the FDA regulations, GCP (Good Clinical Practice) and the International Conference of Harmonization (ICH) guidelines. Over 3000 people have successfully completed our program
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Indian Institute of clinical research & Management, has expanded to provide individuals with additional training options via class room / distance learning system providing flexible and affordable clinical research training via comprehensive training programs, education modules and interactive Webinars. on-site services for institutions in need of clinical research training.

Course Description: PG diploma in clinical research & Management, an interactive program providing distance and classroom training for the clinical research professional, begins with the history of legislation and regulations that govern clinical research and an overview of drug, biologic, and device development. Course participants develop a thorough knowledge base of Good Clinical Practices and International Conference of Harmonization guidelines (E6, E2A), gaining a solid understanding of clinical trial development and management.

The Part 2 classroom training focuses on developing a systematic approach to monitoring, conflict resolution, and problem solving. The participants monitor 6 study subjects and 3 regulatory binders across two study types. Writing effective and professional monitoring reports is also addressed. During the review and discussion of GCP issues, the instructor highlights the differences between device and drug/biologic studies
This course is designed to provide a brief overview of clinical research, terminology, and acronyms followed by a comprehensive review of FDA GCP and ICH GCP (E6). It also reviews the fundamental elements involved in coordinating a clinical trial from the investigator’s perspective. It includes practical tips and suggestions that can be applied to promote a GCP and HIPAA compliant clinical trial, including preventative measures and problem solving techniques of some of the most common GCP non-compliance issues.

Assistance with job placement & resume preparation.