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Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products …

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Number of Students:

906

Created By:

1,499.00

This Course Includes

Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease.
India has been involved in clinical research for a long time and is on the verge of becoming a centre for it. This ever-expanding sector is now looking for competent professionals.
Clinical research is thus a rewarding career option with a lot of room for professional advancement. The average wage range for clinical research specialists in India, according to sources, is between 3 lakhs and 25 lakhs per year!   The online clinical research course from Biogrademy is created with the goal of establishing a firm foundation for clinical research aspirants to build on.  
  • Course Fee: INR 1499/-  (Limited Time Offer)
  • Actual Course Fee: INR 5,700/- (If enrolling after offer)
Bonuses: CV/Resume Preparation + Career Guidance session with career coach.

Eligibility criteria for this program

Pursuing or Pass out students of BSc/BTech or MSc/MTech in Biotechnology, Microbiology, Biochemistry, Chemistry, Pharmaceutical Chemistry. OR BPharm/MPharm The course is open for students from all backgrounds of sciences.  

Major highlights of this program

  • Hard Copy Certificate
  • Recorded videos access for lifetime.
  • CV/Resume Preparation
  • Expert Support

Curriculum

    • 1.1 Introduction Clinical Research 00:18:00
    • 1.2 Evoloution of Clinical Research 00:12:00
    • 1.3 Types of Clinical Research 00:09:00
    • 1.4 Phases of Clinical Research 00:16:00
    • 2.1 Drug Discovery Introduction and History 00:09:00
    • 2.2 Drug Discovery Process 00:14:00
    • 2.3 Pre-Clinical Studies 00:04:00
    • 3.1 Investigational New Drug Application (INDA) 00:07:00
    • 3.2 Types of INDA & Resources of INDA 00:13:00
    • 3.3 Submitting an IND 00:11:00
    • 3.4 Clinical Hold 00:07:00
    • 4.1 Clinical Trials- Phases 00:26:00
    • 4.2 Phase II-IV 00:10:00
    • 5.1 Stakeholders in Clinical Trials 00:14:00
    • 5.2 CRO and RA 00:09:00
    • 5.3 Institutional Review Board 00:04:00
    • 6.1 Clinical Pharmacology 08:00:00
    • 6.2 PK-PD Relationship 00:10:00
    • 6.3 Bioavailability 00:09:00
    • 6.4 Volume of Distribution (Vd) 00:05:00
    • 6.5 Phases of BioTransformation 00:08:00
    • 7.1 Pharmacodynamics 00:07:00
    • 7.2 Drug Action & Factors affecting Drug Response 00:08:00
    • 7.3 Dose Response Curve 00:07:00
    • 7.4 Dose Response Functions, Tolerance 00:05:00
    • 8.1 Pharmacovigilance Introduction 00:17:00
    • 8.2 Pharmacovigilance in India and Terminology 00:10:00
    • 8.3 Pharmacovigilance Process 00:16:00
    • 9.1 Good Clinical Practice, ICH 00:09:00
    • 9.2 Sections and Priciples of GCP-ICH guidelines 00:11:00
    • 9.3 GCP Guidelines- India 00:08:00
    • 9.4 Composition of Ethical Committee 00:09:00
    • 10.1 Ethical Guidelines in Clinical Research 00:09:00
    • 10.2 Universal Ethical Requirements 00:10:00
    • 10.3 Historical Guidelines 00:19:00
    • 11.1 ICMR Introduction 00:09:00
    • 11.2 ICMR Guidelines 00:26:00
    • 11.3 CTRI 00:05:00
    • 11.4 AYUSH and Its Guidelines 00:16:00
    • 12.1 Clinical Data Management (CDM) 00:14:00
    • 12.2 CDM Workflow, Responsibilities of CDM Team 00:13:00
    • 12.3 Study Set Up 00:20:00
    • 12.4 Medical Coding, SAE Reconciliation Quality Check, Database Locking & Advantages of CDM 00:19:00
    • 12.5 Standard Regulations & Guidelines in CDM 00:07:00
    • 12.6 Clinical Data Interchange Standards Consortium 00:07:00
    • 12.7 Collaborative Studies & Quality Analysis , Monitoring 00:14:00
    • 12.8 Data Quality Management (DQM) 00:07:00

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