CLINIMINDS OFFERS YOU TRANSFORM YOUR PROFESSION · GET YOURS WHILE WORKING · MANAGE REGULATORY PROCESS
Batch Commencement: Sunday, 29 January 2023
Advanced Post Graduate Diploma in Drug Regulatory Affairs IPR & Patent
India’s First eSkilling Program in DRA, IPR & Patent Certified by Life Sciences Sector Skill Development Council, National Skill Development Corporation, Ministry of Skill Development & Entrepreneurship, Government of India
Program accredited by Accreditation Council for Clinical Research Edu. ; USA
| Industry Accredited Program | Specialization | Assured Placement Support
| Certified & Accredited by ACCRE, US & PSI of India | LSSSDC Certified
ONLINE E LEARNING PROGRAM LIVE AUDIO VIDEO SESSIONS
Cliniminds Joint venture program with Think i
Demo Session Link: Click Here
Regulatory affairs is a comparatively new profession which developed from the desire of governments to shield public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
Over the course of the last two years, fundamental changes have been made to the format and structure of regulatory affairs regulations, targeting demand and supply disproportion of the healthcare industry. From products, to processes, documentation to services, research to testing, manufacturing to packaging; all aspects of the industry are guarded by set of Govt. regulations.
The pharmaceutical, biotechnology and medical device research and development industries are among the most highly regulated industries globally. As pharmaceutical sector is growing rapidly, there is a need of regulatory affairs professionals to cater the current needs of industries for the global antagonism. Regulatory affairs professionals are the link between pharmaceutical industries and worldwide regulatory agencies. Pharmaceutical industry, being one of the highly regulated industries, is in immense need of people than ever before who are capable of handling issues related to regulatory affairs in a comprehensive manner
Cliniminds has been at the forefront of providing clinical research and pharmacovigilance training and consulting solutions to the life sciences industry for the last several years. We have already trained over 8,500+ professionals. All our programs are internationally accredited.
Triple Certification program:
- Certificate Program in Drug Regulatory Affair IPR & Patent awarded by LSSSDC
- Advanced Post Graduate Diploma in Drug Regulatory Affair IPR & Patent awarded by Cliniminds USA ACCRE
- Internship Certificate awarded by Think I
Benefits with Cliniminds Program:
Live Audio Video Sessions by Experts . Weekends (Saturday & Sunday Classes)
- Internship with Think I
- Pre Placement Training ( CV writing, Mock Interviews , Aptitude Test)
- 24x7 Online access to Learning Management System – Presentations, Notes, Modules, Session Recordings
- Assured Placement Assistance
Program would help you in developing strong understanding of Regulatory Affairs, IPR & Patent
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