ProRelix Education is the Authorized Assessment Centre and Recognized Partner for Up Skilling for “Parakh Se Pehchaan”, an up skilling initiative for experienced professionals by Life Sciences Sector Skill Development Council (LSSSDC), an awarding body for Vocational Qualification under Ministry of Skill Development & Entrepreneurship (MSDE), Govt. of India.
Certification For CRC
Appear for CRC certification exam by LSSSDC and Get your Clinical Research Coordinator NSQF Level 5 Certificate – NSQC approved Vocational Education Qualification Certificate, in 15 days. (Only for experienced clinical research professionals)
It is valid nationally and recognized by top MNCs in India.
Minimum 1 year experience as CRC is compulsory to appear for certification exam.
Contact us at +91 7058895901 for more details.
ProRelix Education announces “Parakh Se Pehchaan”
An initiative by LSSSDC for Experienced Professionals
Appear for Clinical Research Associate NSQF Level 5 certification exam
Under Skill India Mission of MSDE, Govt. Of India
Get your NSQC approved Vocational Education Qualification Certificate for CRA (only for experienced medical and clinical research professionals)
Authorized Assessment Centre and Recognized Partner
for Up Skilling by LSSSDC
FAQ
What is Post Graduate Diploma In Drug Regulatory Affairs?
A Post Graduate Diploma in Drug Regulatory Affairs covers all the topics pertaining to the pharmaceutical drug development process and how they are subject to various degrees of regulation in the market. Some of the topics that you will learn in this module are: ich gcp guidelines, international drug regulations, eCTD submission, and more.
Is Post Graduate Diploma In Drug Regulatory Affairs a good course?
A PG Diploma in Drug Regulatory Affairs can be an exemplary choice for someone who is interested to study the safety and efficacy of pharmaceutical products, medical devices, drug regulations, and etc. As there is a huge demand for trained professionals in this niche, it promises good career growth and plenty of job opportunities which make it a good course to opt for!!
Benefits of pursuing a Post Graduate Diploma In Drug Regulatory Affairs course?
A “Post Graduate Diploma in Drug Regulatory Affairs” is a comprehensive course that revolves around the various aspects and phases of the pharmaceutical regulatory affairs industry. The course is designed to give students insights into the basics as well as the advanced topics such as ICH GCP guidelines, eCTD submission procedure, DMF composing, Dossier preparation and many more. The course focuses on the overall development of the students making them the ideal candidate for lucrative job roles.
Will I get placement assistance after completing this course?
Yes, we oblige into giving students the best opportunities possible but grabbing them and being the best among the others depends on you. Our courses are designed considering the demand of today’s world. Students will be assisted with all the crucial aspects i.e CV building, certification courses, presentation skills, mock interview calls, and much more.