About Course
This is to develop all pharmacy, medical, lifescience background students in the duration of 2 months without attending classroom training.
- Comprehensive syllabus and study material prepared by industry experts.
- Flexibility for multiple specializations like clinical data management programs, Pharmacovigilance programs etc.
- International level training Programs.
- Easy learning solutions.
- Placement program.
- International Level Certificate.
- LMS ID for study material and recorded lectures will be provided.
Benefits of Distance Learning
- You can usually set your own pace of study.
- It is your decision as to when and where you study.
- It doesn’t matter where you live, you can gain a degree from anywhere in the world.
- As with a full-time degree, students may find that they gain useful, transferable skills, such as planning and research.
- A distance learning program costs less than a full-time degree.
List of Courses & Syllabus
| Professional Certificate in | Duration | Modules |
| Clinical Trial | 02 Months | -Fundamentals of Clinical Research -Clinical Research Operations Management |
| Clinical Data Management | 02 Months | -Fundaments of Clinical Data Management -Clinical Research Operations Management |
| ICH-GCP, Ethics & Regulations in Clinical Research | 02 Months | -ICH-GCP, Ethics and Regulations in Clinical Research -Clinical Research Operations Management |
| Pharmacovigilance | 02 Months | -Clinical Research Operations Management -Fundamentals of Pharmacovigilance |
Admission Procedure and Eligibility
Final Written Exam Will Be Conducted And Certificate Will Be Awarded To Successful Candidates Only.
Eligibility
Candidates should be graduated or post graduated in life sciences, pharmacy or medical subjects.
B.Sc/ M.Sc in Life Sciences/ Microbiology/ Biotechnology/ Zoology/ Biochemistry/ Chemistry/ Nursing
B.Pharm/ M.Pharm
BAMS/ BHMS/ BDS/ MBBS/ Physiotherapy.
Admission Procedure
- Download admission form from here
- Fill Admission Form
- Send Photocopy of Self Attested Qualification Documents i.e. Higher secondary (12th) Mark sheet/certificate, Graduation Mark sheet/certificate, 3 Passport Size Photos on Mail
Payment Details
- Google Pay, Phone Pay, Bank Transfer, and NEFT are available call 7058895901 for more details!!
Batches Schedule
Post Graduate Diploma in Clinical Research Distance (PGDCR) – 4 months
| Date | LMS Access Creation Time | Exam | Certificate Issue |
|---|---|---|---|
| After Admission | 01 to 15 days | At the end of 4th month from the date of admission | After Exam |
Professional Certificate in ICH-GCP, Ethics & Regulations In Clinical Research – 2 months
| Date | LMS Access Creation Time | Exam | Certificate Issue |
|---|---|---|---|
| After Admission | 01 to 15 days | At the end of 2nd month from the date of admission | After Exam |
Course Fee
For 3 Months Of Programs
Domestic Students: Rs. 5782/-
International Students: $ 200
FAQ
What is ICH-GCP, Ethics & Regulations In Clinical Research?
ICH GCP, Ethics, and Regulations are the most crucial steps in clinical research. These steps decide if the research is successful or not. Some of the guidelines followed in this process are the rights and well-being of the subject involved in a clinical trial, protocols, accurate reporting, handling of data, and more.
Is ICH GCP a good course?
In this course, you will learn various ethics and regulations of different countries regarding clinical research, fundamentals of research, operational knowledge, clinical management, and more. It is an excellent choice if you want to have a global career in the domain of clinical research, as determining the efficacy of products developed is a very meaningful and demanding job.
Benefits of pursuing a ICH GCP course?
The ICH GCP course is a must-have certification for those looking to start careers in clinical research, pharmacovigilance, and clinical trials. Without these guidelines, it is impossible to conduct successful research with reliable and high-quality data. This course will teach you all of the regulations that should be followed for any type of clinical research, such as the Helsinki Declaration, the well-being of the trial subject, the subject’s rights, and more. By pursuing a career in ICH-GCP one can achieve many milestones and land up prestigious global opportunities in the field.
Job opportunities after completing ICH GCP course?
After successfully completing the Professional Clinical Trial course, you will have a variety of options. You will be adequately qualified for a variety of jobs such as Clinical Trial Manager, Clinical Trial Monitor, Clinical Research Coordinator, etc. Conducting clinical trials is not a one-person job and thus necessitates the recruitment of disciplined and adaptive personnel in the industry.
