Advanced Post Graduate Diploma in Clinical Research & Regulatory Affairs in Pharma & Clinical Research

Post Graduate Diploma

In Noida

₹ 30,500 VAT incl.

Description

  • Type

    Post Graduate Diploma

  • Location

    Noida

  • Duration

    6 Months

  • Start date

    Different dates available

Regulatory professionals are the primary communication link between the company and global regulatory
agencies such as USFDA (United States Food and Drug Administration) and European Union of Drug
Regulatory Affairs (EUDRA).

Facilities

Location

Start date

Noida (Uttar Pradesh)
See map
C-101, 1st Floor, Sector 2, Noida 201301, 201301

Start date

Different dates availableEnrolment now open

About this course

Course Objectives
• To provide a comprehensive introduction to the clinical research process.
• Learn the skills, knowledge and competencies of a candidate for the Clinical Research jobs.
• Become more familiar with roles/jobs as part of the study team.
• Concepts and importance of Drug Regulatory Guidelines
• Learn the skills, knowledge and competencies of a candidate for the drug regulatory jobs.
• Become more familiar with roles/jobs as part of the regulatory affairs team.
• Understanding of all drug development, marketing and post marketing regulatory issues.

MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B.Pharms, Graduate/Post
Graduate Degree in Life Sciences, Mathematics, Pharmacology, Pharmacy, Medical
Laboratory, Nursing, Biochemistry, Microbiology, Biotechnology and all professionals
working with Pharmaceutical companies, CROs and Hospitals.

MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B.Pharms, Graduate/Post
Graduate Degree in Life Sciences, Mathematics, Pharmacology, Pharmacy, Medical
Laboratory, Nursing, Biochemistry, Microbiology, Biotechnology and all professionals
working with Pharmaceutical companies, CROs and Hospitals.

MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B.Pharms, Graduate/Post
Graduate Degree in Life Sciences, Mathematics, Pharmacology, Pharmacy, Medical
Laboratory, Nursing, Biochemistry, Microbiology, Biotechnology and all professionals
working with Pharmaceutical companies, CROs and Hospitals.

Placement support would be provided to the successful candidates. CVs of successful candidates would be forwarded to relevant organization.

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Subjects

  • Bsc
  • Msc
  • MBBS
  • BDS
  • BHMS
  • BAMS
  • BUMS
  • BPT
  • B.Pharms
  • Mathematics
  • Pharmacology
  • Pharmacy
  • Medical Laboratory
  • Nursing
  • Biochemistry
  • Microbiology
  • Biotechnology

Teachers and trainers (1)

Joseph Mathew

Joseph Mathew

Subject-Matter Expert on Pharmacovigilance

Course programme

Clinical Research Introduction• Principles of Pharmacology & Drug Discovery & Development• Roles & Responsibilities of Key Stakeholders• Preparations & Planning for Clinical Trials• Essential Documentation in Clinical Research & Regulatory Submissions• Clinical Trials Project Planning & Management• Study Start Up Process• Clinical Monitoring Essentials• Compliance, Auditing & Quality Control in Clinical Research• Overview of Clinical Data Management and Pharmacovigilance

Advanced Post Graduate Diploma in Clinical Research & Regulatory Affairs in Pharma & Clinical Research

₹ 30,500 VAT incl.