MSc-PGDip in Clinical Pharmacology and PGCert in Clinical Research

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University of Surrey

Comments about MSc-PGDip in Clinical Pharmacology and PGCert in Clinical Research - At the institution - Guildford - Surrey

• Objectives
  Clinical Pharmacology is a medical scientific discipline concerned with the study of therapeutic or diagnostic chemical substances to help establish the theoretical and practical basis for their rational clinical application. A full understanding of the pharmacodynamic and pharmacokinetic behaviour optimises evaluation in therapeutic clinical trials and post-registration use in the treatment and/or diagnosis of disease. The awards qualify an individual as having received postgraduate training suitable for senior scientific and clinical posts within clinical pharmacology. The programme is designed to: -Give a greater understanding of clinical pharmacology -Provide evidence of specialisation, which is increasingly required under EU legislation -Demonstrate proficiency across the whole field of clinical pharmacology through a system of continuous assessment -The programme enables you to gain a wider perspective and the critical evaluation skills relating to medicine design and conduct of clinical trials (nationally and internationally). The part-time and modular nature of the programme is well suited to busy people with additional work commitments, allowing a flexible rate of attendance (one to four modules per year).
• Academic title
  MSc/PGDip in Clinical Pharmacology and PGCert in Clinical Research
• Course description
  MSc/PGDip in Clinical Pharmacology and PGCert in Clinical Research Module overview
  
  Programme Orientation and Principles of Drug Development
  This module is an introductory overview of the drug development process 'from molecule to medicine' and the healthcare environment within which the pharmaceutical industry operates.
  
  Pre-clinical Discovery and Development of New Medicines
  This module considers the early stages in the drug development process, from research strategy to lead candidate identification, including the methodology used in establishing the toxicological profile of new drug candidates and predicting drug safety in man.
  
  Regulatory Affairs*
  This module covers the systems adopted by government authorities for regulating safety, efficacy and quality of medicines during the development and marketing of new drugs.
  
  Clinical Development and Therapeutics*
  This module considers the principles of clinical research in clinical trial design, implementation, evaluation and reporting on Phase II-IV studies across many therapeutic areas.
  
  Healthcare Marketplace
  This module looks at the healthcare environment in which the commercial development of drugs takes place, including strategic, financial and operational planning, marketing, sales and promotion.
  
  Pharmacokinetics and Drug Absorption, Distribution, Metabolism and Excretion
  This module covers pharmacokinetic analysis from sample collection through mathematical data analysis to interpretation of results. Factors affecting absorption, distribution, metabolism and excretion of a drug and their assessment in animals and man are looked at.
  
  Clinical Pharmacology and Non-patient Volunteer Study Design
  This module considers the types of clinical pharmacology study and their implementation, and the legal, ethical, moral and regulatory requirements of study design in healthy human volunteer subjects.
  
  Drug Safety
  This module considers all aspects of safety monitoring, signal detection, study design, appraisal of safety issues, crisis management and communication.
  
  Ethical and Legal Aspects
  This module looks at the legal and ethical requirements for conduct of clinical research, with an emphasis on regulatory control.
  
  Translational Medicine and Biomarkers
  This module explores the non-invasive methods used in healthy volunteers in decision making, the design of efficacy and safety studies in patients, and how these findings can be translated into the drug development programme.
  
  Pharmacoeconomics
  This module considers the key concepts underpinning pharmacoeconomic evaluations at different stages in the drug development process.
  
  Research Methods
  This module covers the practical approaches to understanding and conducting research in the pharmaceutical sector including study design, methodology and evaluation, including statistical principles and reporting.
  
  * Modules validated by the Faculty of Pharmaceutical Medicine for Specialist Training purposes
  
  Typical entry requirements
  A degree (medical or non-medical) or professional qualifications and/or practical experience sufficient to satisfy the Head of Department and the Programme Directors of the applicant's ability to pursue the programme of study.
  
  Selection is based upon the candidate's application and references. An informal interview may be required.
   
  Programme length
  4-8 modules over 24-72 months part-time/distance learning.
  

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