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University of Bradford: Drug Toxicology and Safety Pharmacology
| Institution | University of Bradford |
|---|---|
| Department | School of Pharmacy and Medical Sciences |
| Web | http://www.bradford.ac.uk |
| admissionslife@bradford.ac.uk | |
| Telephone | 01274 236088 |
| Study type | Taught |
MSc
Summary
This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.
It addresses key aspects of preclinical drug evaluation through the study of:
- Drug discovery and development
- Safety pharmacology
- Mechanisms of drug-induced toxicities
- Regulatory affairs
- Bioanalytical sciences
It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.
As part of the programme you will undertake an original research project that will be the basis of your dissertation.
Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.
Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.
Rankings
We are ranked in the top 250 universities in the world for Pharmacy & Pharmacology in the 2019 QS World University Rankings by subject.
| Level | RQF Level 7 |
|---|---|
| Entry requirements | A 2.2 Honours degree or above in a related scientific discipline e.g. biosciences, chemistry, biomedical, medical, pharmaceutical, pharmacological, or toxicological studies; applications are also welcome from candidates with non standard qualification, with significant relevant experience. IELTS at 6.0 or the equivalent. |
| Location | Main Site Richmond Road Bradford BD7 1DP |
Fees
| England | 9230 GBP for Whole course |
|---|---|
| Northern Ireland | 9230 GBP for Whole course |
| Scotland | 9230 GBP for Whole course |
| Wales | 9230 GBP for Whole course |
| Republic of Ireland | 9230 GBP for Whole course |
| EU | 23028 GBP for Whole course |
| International | 23028 GBP for Whole course |
| Channel Islands | 23028 GBP for Whole course |
Summary
This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.
It addresses key aspects of preclinical drug evaluation through the study of:
- Drug discovery and development
- Safety pharmacology
- Mechanisms of drug-induced toxicities
- Regulatory affairs
- Bioanalytical sciences
It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.
As part of the programme you will undertake an original research project that will be the basis of your dissertation.
Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.
Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.
Rankings
We are ranked in the top 250 universities in the world for Pharmacy & Pharmacology in the 2019 QS World University Rankings by subject.
| Level | RQF Level 7 |
|---|---|
| Entry requirements | A 2.2 Honours degree or above in a related scientific discipline e.g. biosciences, chemistry, biomedical, medical, pharmaceutical, pharmacological, or toxicological studies; applications are also welcome from candidates with non standard qualification, with significant relevant experience. IELTS at 6.0 or the equivalent. |
| Location | Main Site Richmond Road Bradford BD7 1DP |
Fees
| England | 9230 GBP for Whole course |
|---|---|
| Northern Ireland | 9230 GBP for Whole course |
| Scotland | 9230 GBP for Whole course |
| Wales | 9230 GBP for Whole course |
| Republic of Ireland | 9230 GBP for Whole course |
| EU | 23028 GBP for Whole course |
| International | 23028 GBP for Whole course |
| Channel Islands | 23028 GBP for Whole course |
Summary
This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.
It addresses key aspects of preclinical drug evaluation through the study of:
- Drug discovery and development
- Safety pharmacology
- Mechanisms of drug-induced toxicities
- Regulatory affairs
- Bioanalytical sciences
It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.
As part of the programme you will undertake an original research project that will be the basis of your dissertation.
Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.
Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.
Rankings
We are ranked in the top 250 universities in the world for Pharmacy & Pharmacology in the 2019 QS World University Rankings by subject.
| Level | RQF Level 7 |
|---|---|
| Entry requirements | A 2.2 Honours degree or above in a related scientific discipline e.g. biosciences, chemistry, biomedical, medical, pharmaceutical, pharmacological, or toxicological studies; applications are also welcome from candidates with non standard qualification, with significant relevant experience. IELTS at 6.0 or the equivalent. |
| Location | Main Site Richmond Road Bradford BD7 1DP |
Fees
| England | 9004 GBP for Whole course |
|---|---|
| Northern Ireland | 9004 GBP for Whole course |
| Scotland | 9004 GBP for Whole course |
| Wales | 9004 GBP for Whole course |
| Republic of Ireland | 9004 GBP for Whole course |
| EU | 21930 GBP for Whole course |
| International | 21930 GBP for Whole course |
| Channel Islands | 21930 GBP for Whole course |
Master of Research - MRes
Summary
This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.
It addresses key aspects of preclinical drug evaluation through the study of:
- Drug discovery and development
- Safety pharmacology
- Mechanisms of drug-induced toxicities
- Regulatory affairs
- Bioanalytical sciences
It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.
As part of the programme you will undertake an original research project that will be the basis of your dissertation.
Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.
Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.
| Level | RQF Level 7 |
|---|---|
| Entry requirements | 2:1 or above Honours degree in Biological Sciences, Chemical Sciences, Pharmacy, Pharmacology or Pharmaceutical Sciences. Candidates with a 2:2 Honours degree and relevant experience will be considered on an individual basis. English language requirements: IELTS at 6.0 or equivalent level qualification |
| Location | Main Site Richmond Road Bradford BD7 1DP |
Fees
| England | 9230 GBP for Whole course |
|---|---|
| Northern Ireland | 9230 GBP for Whole course |
| Scotland | 9230 GBP for Whole course |
| Wales | 9230 GBP for Whole course |
| Republic of Ireland | 9230 GBP for Whole course |
| EU | 23028 GBP for Whole course |
| International | 23028 GBP for Whole course |
| Channel Islands | 23028 GBP for Whole course |
Summary
This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.
It addresses key aspects of preclinical drug evaluation through the study of:
- Drug discovery and development
- Safety pharmacology
- Mechanisms of drug-induced toxicities
- Regulatory affairs
- Bioanalytical sciences
It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.
As part of the programme you will undertake an original research project that will be the basis of your dissertation.
Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.
Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.
| Level | RQF Level 7 |
|---|---|
| Entry requirements | 2:1 or above Honours degree in Biological Sciences, Chemical Sciences, Pharmacy, Pharmacology or Pharmaceutical Sciences. Candidates with a 2:2 Honours degree and relevant experience will be considered on an individual basis. English language requirements: IELTS at 6.0 or equivalent level qualification |
| Location | Main Site Richmond Road Bradford BD7 1DP |
Fees
| England | 9230 GBP for Whole course |
|---|---|
| Northern Ireland | 9230 GBP for Whole course |
| Scotland | 9230 GBP for Whole course |
| Wales | 9230 GBP for Whole course |
| Republic of Ireland | 9230 GBP for Whole course |
| EU | 23028 GBP for Whole course |
| International | 23028 GBP for Whole course |
| Channel Islands | 23028 GBP for Whole course |
Summary
This full-time Master's programme provides a comprehensive overview of drug safety practices within the drug development process.
It addresses key aspects of preclinical drug evaluation through the study of:
- Drug discovery and development
- Safety pharmacology
- Mechanisms of drug-induced toxicities
- Regulatory affairs
- Bioanalytical sciences
It will give you state-of-the-art training in preclinical toxicology, with an emphasis on the molecular in vitro and in vivo aspects of toxicology and safety pharmacology assessments.
As part of the programme you will undertake an original research project that will be the basis of your dissertation.
Delivered at the Institute of Cancer Therapeutics, an internationally renowned research institution, the programme gives you the skills you need for a career in the pharmaceutical industry or regulatory bodies, along with the foundations for PhD study.
Drug toxicology and safety pharmacology lies at the heart of the chemical and pharmaceutical industries, and demand for highly skilled practitioners in this field is extremely high.
| Level | RQF Level 7 |
|---|---|
| Entry requirements | 2:1 or above Honours degree in Biological Sciences, Chemical Sciences, Pharmacy, Pharmacology or Pharmaceutical Sciences. Candidates with a 2:2 Honours degree and relevant experience will be considered on an individual basis. English language requirements: IELTS at 6.0 or equivalent level qualification |
| Location | Main Site Richmond Road Bradford BD7 1DP |
Fees
| England | 9004 GBP for Whole course |
|---|---|
| Northern Ireland | 9004 GBP for Whole course |
| Scotland | 9004 GBP for Whole course |
| Wales | 9004 GBP for Whole course |
| Republic of Ireland | 9004 GBP for Whole course |
| EU | 21930 GBP for Whole course |
| International | 21930 GBP for Whole course |
| Channel Islands | 21930 GBP for Whole course |
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