-
All
-
Online
-
Filters
-
Location
-
Online
-
Type of studies
-
+ Filters
Regulatory affairs courses
- GCSE
- Online
- Different dates available
- 6 Months
...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Regulatory Affairs and Safety, Drug Trial, Drug Interaction...
- Course
- Online
- Different dates available
- 6 Months
...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Mobile Engineering, Mobile Marketing, Clinical Study...
- GCSE
- Online
- Different dates available
- 1 Year
...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Drug Designing, Drug Trial, Drug Counselling...
- Course
- Online
- Different dates available
- 6 Months
...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Drug Trial, Drug Interaction, Drug Development...
- Course
- Online
- Different dates available
- 6 Months
...Module I : Fundamentals of Clinical Trials Module II : Drug Development Module III : Conduct of Clinical Research Module IV : Regulatory Affairs... Learn about: Technology Education, Operating turbines and alternators, Drug Development...
- HNC
- Online
- Different dates available
- 1 Year
...CONCEPTS MARKETING PLANNING & SEGMENTATION MARKETING OF SERVICE INDUSTRIAL MARKETING SERVICES MARKETING PROJECTS... Learn about: Fundamentals of Clinical Trials, Agricultural Science, Agricultural Sciences...
- HNC
- Online
- Different dates available
- 2 Years
...& Biosystematics(core)4Micro-104Biostatistics & bioinformatics** (Multidisciplinary/Interdisciplinary)5Micro-105Combined pactical couse6Micro-106Seminar course... Learn about: Education School, Clinical Psychology, Multimedia Graphics...
- Short course
- Navi Mumbai (India)
- Different dates available
- 2 Months
...BETWEEN 12K TO 25K 2) CABIN CREW Job duties of cabin crew The role of an air cabin crew member is to provide excellent customer service to passengers while... Learn about: Drug Development, Regulatory Affairs and Safety, Fundamentals of Clinical Trials...
- HNC
- Online
- Different dates available
- 2 Years
...1Second Semester1Micro-207Biochemistry(core)2Micro-208Biotechnology & immunology(core)3Micro-209Environmental science... Learn about: IT industry, Care Management, NUTRITION FOOD VALUE...
- Course
- (Harrington Hall Hotel, London)
- 2 Days
...This seminar will provide a comprehensive overview of the requirements for successful product approval for medical devices in Latin America. The programme will cover the regulatory requirements but will also share the interpretation of the regulation, guidance and legislation in these countries...
- Course
- Intermediate
- 2 Days
...This seminar will provide you with an essential overview of the key areas of Pharmaceutical regulatory affairs in the Middle East. This two day course will focus on practical aspects to assist with regulatory affairs in the region. The course will include interactive discussion sessions to allow...
- Short course
- (The Rembrandt Hotel, London)
- 1 Day
...This Course provides an introduction to Support Staff in Regulatory Affairs and elsewhere about most of the basics of drug development, including information, how companies can apply for approvals in Europe and the US, dealing with the national agencies and the EMEA. Suitable...
- Course
- (Harrington Hall Hotel, London)
- 2 Days
...This is a comprehensive seminar designed for all those needing to learn about recent and expected regulatory developments in the countries to be covered, to assist with future marketing authorisation applications and in-market regulatory compliance. Suitable for: Anyone in the pharma industry...
- Course
- (The Rembrandt Hotel, London)
- 2 Days
...This course will provide you with an understanding of the basics of EU Regulatory Affairs and the EU legislative framework. Key topics will be covered and strategies discussed to help you improve your regulatory affairs activities and optimise your drug submission procedures. Suitable...
-
I’ve learnt a lot about "Regulatory affairs". Thank you for your great support and motivation to pass the exam.
← | →
- Postgraduate
- Blended
...Emagister.co.uk has just added this course on regulatory affairs (frequently called government affairs) to its catalogue. It is a profession than entails regulated industries regarding healthcare service, banking, energy, etc. Global regulatory agencies are as USFDA (United States Food and... Learn about: Medical training, Drug Development, CLINICAL TRIALS...
...Emagister.co.uk has just added this course on regulatory affairs (frequently called government affairs) to its catalogue. It is a profession than entails regulated industries regarding healthcare service, banking, energy, etc. Global regulatory agencies are as USFDA (United States Food and... Learn about: Medical training, Drug Development, CLINICAL TRIALS...
-
I’ve learnt a lot about "Regulatory affairs". Thank you for your great support and motivation to pass the exam.
← | →
- Course
- Bedfordshire
...Why this course? This part-time course provides graduate professionals working in healthcare regulatory affairs or related areas, who have already... Learn about: Medical training...
- Short course
- Bedfordshire
... and Japan Critically evaluate the skills and competencies required by the regulatory affairs professional in managing a department including, communication... Learn about: Strategic Management...
- Short course
- Bedfordshire
... Demonstration of conformity through pre-clinical bench testing and clinical evaluation Introduction to the central role of risk assessment in regulatory affairs... Learn about: Medical training...
- Postgraduate
- Blended in Ahmadābād (India)
... and other resources that are deemed by the competent authority to be related to the clinical trial and that may be located at the trial site, at the sponsor and/or contract research organisation’s facilities or at other establishments deemed appropriate by the Regulatory Authority.” This program deals... Learn about: Clinical Research, Regulatory Affairs, Quality Assurance...
- Course
- Chicago (USA)
- Advanced
- 2 Days
...; Electronic Signatures. In the past FDA used to issue several Warning Letters to the same firms upon consecutive inspections. Today, after receiving one Warning Letter the next regulatory action is elevated to Import Alert, Consent Decree, and Injunctions for domestic manufacturers... Learn about: Pharmaceutical laboratory administration, Food safety, FDA perspective...