REGULATORY AFFAIRS, IPR & PATENT
Global Institute of Health Science is a pioneer in health science education especially in distance & online education. Global Institute of Health Science is an ISO 21001:2018 Certified health science Institute & globally acclaimed, also certified with copyright approval from IPR Government of INDIA. GIHS have international certification from UASL UK for Quality Control Management System.
WHY CHOOSE US
Regulatory affairs (RA), also called government affairs, are a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking.
Regulatory affairs also have a very specific meaning within the healthcare industries globally and professionals can be recruited in Pharma companies, medical devices, biotech, biologics and functional food areas.
It deals with government or law. Global regulatory agencies are as USFDA (United States Food and Drug Administration) and European Union of Drug Regulatory Affairs (EUDRA).
This Program is developed to prepare professionals for regulatory affairs positions in the pharmaceutical, biopharmaceutical and medical device industries i.e. to facilitate them with the educational foundation that will support them advance in the regulatory affairs profession.
The program will provide the students with the fundamentals required in both regulatory affairs and quality operations.
SYLLABUS
Regulatory Affairs
Pharmaceutical Legislation in India
Pharmaceutical Regulation Process in India
Regulation of Generic Pharmaceutical and Bio Similar Product
Introduction to USFDA
Regulatory affairs (RA), also called government affairs, are a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking. Regulatory affairs also have a very specific meaning within the healthcare industries globally and professionals can be recruited in Pharma companies, medical devices, biotech, biologics and functional food areas. It deals with government or law. Global regulatory agencies are as USFDA (United States Food and Drug Administration) and European Union of Drug Regulatory Affairs (EUDRA).
The GIHS Program is developed to prepare professionals for regulatory affairs positions in the pharmaceutical, biopharmaceutical and medical device industries i.e. to facilitate them with the educational foundation that will support them advance in the regulatory affairs profession. The program will provide the students with the fundamentals required in both regulatory affairs and quality operations. This course is designed to give industry level education in field of legal and regulatory issues. The program focuses on regulatory affairs concept which the Pharma companies must comply to sell their drugs both domestically and in the international market. Pharmaceutical regulatory affairs courses in Healthcare Industry is related to IPR (Intellectual Property Rights), Patents, copyrights and Trademarks with quality standards. We provide degree certified regulatory affairs courses, IPR certificate course in India.
*Fees subject to taxes & exchange rates.
*Fees subject to taxes & exchange rates.
Trustindex verifies that the original source of the review is Google. Amazing institute.Very helpful and supportive team. I had a beautiful learning experience.Posted on Google Sireesha VegesnaTrustindex verifies that the original source of the review is Google. I liked that Ijoined with the best countries by your Helping ProcessPosted on Google balvir singhTrustindex verifies that the original source of the review is Google. The PG Diploma in Nutrition course covers the basic concepts clearly. Teaching is satisfactory and the study material is useful for understanding nutrition fundamentals. Overall, it is a decent course for those looking to gain knowledge in this field.Posted on Google Samridhi SharmaTrustindex verifies that the original source of the review is Google. Vijay sir and chethan sir Thanks for your guidance throughout the academic year. May God bless this institute even more!Posted on Google Sobhiya ParuthiTrustindex verifies that the original source of the review is Google. Very goodPosted on Google Santosh DsouzaTrustindex verifies that the original source of the review is Google. One of the best institutions. I have recently completed my PG Diploma in Clinical Research and Pharmacology. Course is carefully structured and detailed. Management is very well organised and prompt in assistance. I would highly recommend this institution.Posted on Google A V
Medical radiology technology involves the use of medical imaging equipment such as X-rays, CT scans, MRIs, and ultrasound to create detailed images of the internal structures of the body. This imaging is done to assist in the diagnosis and treatment of medical conditions.
Quality management in radiology involves implementing processes and standards to ensure the accuracy, safety, and effectiveness of radiologic procedures.
To become a radiology manager, you may need a bachelor’s degree in radiologic technology or any related field. You can then pursue additional certifications in management and gain relevant experience.
Quality assurance (QA) and quality control (QC) in radiology involve systematic processes to ensure the reliability and accuracy of radiologic imaging. QA focuses on continuous improvement and adherence to standards, while QC focuses on routine checks and tests to maintain equipment performance.
The scope of radiology management includes overseeing the operation of radiology departments, ensuring compliance with safety and quality standards, managing personnel, budgeting, implementing new technologies, and collaborating with healthcare professionals.





















































