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Drug regulatory affairs courses
- Certificate
- Online
- Different dates available
- 6 Months
...Drugs are developed with the intention of providing maximum benefits to patients with minimum of adverse effect. A Clinical research study in human volunteers answers to specific health questions. Carefully conducted clinical trials are the fastest and safest way to find treatments that... Learn about: Clinical Trial, Fundamentals of Clinical Trials, Drug Development...
- Post Graduate Diploma
- Online
- 1 Month
... to Pharmaceutical Industry & Global Challenges - Ethical Consideration in Clinical Trials - Global Clinical Research Environment & Opportunities - Regulatory Affairs...
- Master
- Pune
- 2 Years
... Environment Organisational Effectiveness & Change Indian & International Regulatory Affairs Essential Document Writing Semister - III Entrepreneurship...
- Bachelor
- Pune
... Jurisprudence & Regulatory Affairs...
- Post Graduate Diploma
- Hyderabadandanother venue.
- Bhopal
- 1 Year
... to Pharmaceutical Industry & Global Challenges - Ethical Consideration in Clinical Trials - Global Clinical Research Environment & Opportunities - Regulatory Affairs...
- Bachelor
- Pune
...) Pharmaceutical Jurisprudence & Regulatory Affairs...
- Certificate
- Online
- 6 Months
...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: Practice and Procedure, Industrial IPR Design &Trademark, IT Industry...
- Certificate
- Online
- 6 Months
...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: IT Industry, Industrial IPR Design &Trademark, Regulatory Compliance...
- Certificate
- Online
- 6 Months
...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: Intellectual Property, Industrial IPR Design &Trademark, IT Industry...
- Certificate
- Online
- 6 Months
...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: Industrial IPR Design &Trademark, International Rights, IT Industry...
- Certificate
- Online
- 6 Months
...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: Intellectual Property, IT Industry, Control system...
- Certificate
- Online
- 6 Months
...The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs... Learn about: Intellectual Property, Industrial IPR Design &Trademark, Practice and Procedure...
- Course
- Online
- 6 Months
...Drugs are developed with the intention of providing maximum benefits to patients with minimum of adverse effect. A Clinical research study in human volunteers answers to specific health questions. Carefully conducted clinical trials are the fastest and safest way to find treatments that... Learn about: Clinical Studies, Clinical Research, Clinical Trial...
- Certificate
- Bangalore
- 3 Months
.../Independent Ethics Committee (IRB/IEC) - Process of ethical approval - Informed consent Regulatory Affairs & Marketing Approval - Drugs and Cosmetics Act...
- PhD
- Online
- 3 Years
.... Regulatory Affairs in Clinical Trials 9. Bioethics – Ethical Aspects of Clinical Trials 10. Clinical Data Management 11. Pharmacovigilance and Safety...
- Master
- New Delhi
- 18 Months
... Trials 8. Regulatory Affairs in Clinical Trials 9. Bioethics – Ethical Aspects of Clinical Trials 10. Clinical Data Management 11. Pharmacovigilance...