PgDip Pharmacovigilance

Postgraduate

In Hatfield

£ 1,350 VAT inc.

Description

  • Type

    Postgraduate

  • Location

    Hatfield

  • Duration

    2 Years

  • Start date

    Different dates available

The PGDip Pharmacovigilance is a course developed by the School of Life and Medical Sciences at the University and the Pharmaceutical Information and Pharmacovigilance Association (PIPA). On this course you will study relevant techniques used in pharmacovigilance including the basis of adverse drug reactions, regulations and guidelines (UK, EU and major worldwide regions), handling safety issues including Labelling and Risk Management Systems and processes (both pre and post-marketing).

Facilities

Location

Start date

Hatfield (Hertfordshire)
See map
De Havilland Campus, Mosquito Way

Start date

Different dates availableEnrolment now open

About this course

Potential candidates will normally be in either full or part-time employment and are likely to have a spread of responsibilities, mostly in pharmacovigilance and medical information, monitoring safety data in either pre- and post-marketing studies or from spontaneous reports. They will be graduates and/or experienced personnel and usually will have held positions in drug safety for one to several years. Some applicants may have doctorates and may be medically qualified. Following successful completion of the course the knowledge gained should enable the post-graduates to make a greater contribution to the pharmacovigilance industry.

A first or second class honours degree in biosciences, chemical sciences or pharmacy or an equivalent professional qualification in veterinary science, medicine or dentistry. Applicants with other qualifications, research publications or relevant drug safety experience will be considered individually. Plus at least 6 months experience in full time employment in a pharmacovigilance workplace.

This course is accreditated by the PIPA (Pharmaceutical Information and Pharmacovigilance Association)

Why choose this course?
Expertise of the staff, who are experienced professionals and have real world expertis in pharmacovigilance from the pharmaceutical industry and regulatory authorities
Flexibility of study, based on intensive three-day taught courses with independent
Pre and post coursework activities
Practical research projects based on real-world situations
Opportunities for sharing experiences and networking which contributes to the

Questions & Answers

Add your question

Our advisors and other users will be able to reply to you

Who would you like to address this question to?

Fill in your details to get a reply

We will only publish your name and question

Reviews

This centre's achievements

2020

All courses are up to date

The average rating is higher than 3.7

More than 50 reviews in the last 12 months

This centre has featured on Emagister for 6 years

Subjects

  • Risk
  • Risk Management
  • Systems
  • IT risk
  • Regulations
  • Knowledge
  • Ability
  • Presentations
  • Essays
  • Coursework

Course programme

What will I study?

Taught modules normally consist of approximately 24 hours class contact. In addition, about 120 hours will be needed to complete the pre and post-course activities. The actual amount of time spent will depend upon your existing knowledge and ability. All modules are free-standing. Satisfactory completion of four modules is compulsory for the PgCert; all eight modules are required for the PgDip and MSc. Coursework will contribute significantly to assessment and may comprise some or all of the following: summaries of pre-course reading, written reports of class discussions, essays, performances in seminars, poster presentations, problem solving or data interpretation exercise, short projects and case studies. Unseen written examinations will feature in some courses; they may be used to examine understanding of pre-course reading material. Attendance at the taught component and satisfactory completion of both coursework and examinations (where present), with a minimum mark of 50% in each element, is normally required to pass each module.

Level 7

Module
  • Pharmacovigilance Regulations and Guidelines
  • Drug Safety in Clinical Trials
  • Adverse Drug Reactions by Major Body Systems II
  • Management of Pharmacovigilance Data
  • Principles of Pharmacovigilance
  • Adverse Drug Reactions by Major Body Systems I
  • Pharmacoepidemiology
  • Labelling and Risk Management

Additional information

Fees 2021

UK Students

Part time
£1350 per 15 credits for the 2021/2022 academic year

EU Students

Part time
£1350 per 15 credits for the 2021/2022 academic year

PgDip Pharmacovigilance

£ 1,350 VAT inc.