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Tuesday, June 27, 2017
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Accredited Online Training Programs

CPD Accredited TrainingMany of the dinaris.org’s professional clinical research, regulatory affairs, and drug safety training programs are are accredited, and offer Continuing Professional Development (CPD) points by the Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians of the United Kingdom.

On completion of each course, learners earn CPD points in proportion to the course’s duration. The CPD points earned are specified on the certificate awarded to the learner on successful completion of the course’s multiple-choice-question assessment.

Below you will find a list of the courses which offer these CPD point upon completion.

CPD points for Accredited Training Courses

BP ID

CPD ID

Title

CPD points

GCP020

CT01

How to Gain Approval to Conduct Clinical Trials in
Europe

3

GCP001

CT03

An Introduction to ICH Good Clinical Practice

3

GCP002

CT04

An Introduction to Clinical Trial Preparation and Design

4

GCP004

CT06

Clinical Trial Monitoring: Site Evaluation and Set-up

1.5

GCP003

CT07

An Introduction to Clinical Trials and Drug Development

1.5

GCP005

CT08

Clinical Trial Monitoring: Study Monitoring, Documentation
and Closure

2

GCP006

CT09

Good Clinical Practice Inspections and Audits

2.5

GCP007

CT10

The Investigational New Drug Application (IND) to Conduct
FDA-regulated Clinical Trials

3

PRA01

ESS01

Essentials of EU and US Regulatory Affairs for Human
Medicinal Products

3

DS001

PV03

An Introduction to Drug Safety and Pharmacovigilance

2

NA

QAC01

An Introduction to Good Quality Control Laboratory
Practice

2

NA

SC01

Pharmacokinetics and Pharmacodynamics in Drug Registration

3.5

PRA02

SUB01

Orphan Drug Designation in the USA and Europe

1.5

PRA20

SUB02

The European Centralised Procedure (CP)

1.5

PRA21

SUB03

The Mutual Recognition Procedure (MRP)

2

PRA03

SUB04

Preparing Submissions in the Common Technical Document
(CTD) Format

1.5

PRA04

SUB05

Electronic Common Technical Document (eCTD)

2.5

PRA22

SUB06

Variations to Marketing Authorisations in Europe

3.5

PRA005

SUB07

Registration of Monoclonal Antibodies

3

PRA06

SUB08

How to Gain Approval to Market a Generic Medicinal
Product in the USA

3.5

PRA07

SUB09

The New Drug Application (NDA) for Marketing Approval
in the USA

3.5

PRA23

SUB11

The Decentralised Procedure (DCP)

2

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