Clin Infotech

Teacher Name

35 Days

Regualatory Affairs Course Certification Training

Clininfotech offers a comprehensive Regulatory Affairs Course training that will help you master fundamentals, advanced theoretical concepts like Regualtory  operations in Formulation and Medical Device Pharmaceutical Industry while getting hands-on practical experience with the functional applications as the training is blended with hands on assignments and live projects.

Get Industry ready with Dedicated Career Support

Clininfotech offers Regulatory Affairs Course  for beginners to advanced level with high quality Industry Experience Trainers with extensive training experience and considered to be the best in the industry  and  projects will be provided as Part of the Regulatory Affairs Course to ensure hands-on experience. Participants can Get the Regulatory Affairs Certification Course at the end of the training.

Who Should Do Regulatory Affairs Course?

Regulatory Affairs course is well suited for the participants at all levels of Pharmacy Freshers and  Experience Pharmaceutical Employees. This course is best suited for the Professionals who can consider Regulatory Affairs Career as a next logical move to enhance in their careers include:

  • Pharmacy Professionals ( B.Pharamcy / M.Pharamacy / Pharm D)  from any domain who has Good analytical skills
  • Medical Professionals (MBBS / BDS/ BPT/ BHMS/BAMS/ Nursing) Freshers / Experience Professionals.
  • sc / M.Sc ( Biotech/ Microbiology/ Biochemisty/ Chemistry & All Life Sciences) Freshers / Expereince
  • Software programmers
  • Business analysts
  • Six Sigma consultants
  • Fresher from any Science stream with good Analytical and logical skills

Interview Preparation Sessions

Participants who have completed the Regulatory Affairs course training and the projects will be put under our Placement Incubation Program. As part of this program, participants will undergo a thorough interview preparation process on Clinical Research. A huge repository of Regulatory Affairs Interview questions with answers will be provided for the participants to prepare. A dedicated Regulatory Affairs Subject Matter Expert (SME) will help in resume building, conduct mock interviews and evaluate each participant’s knowledge, expertise and provide feedback. Our SMEs will do the necessary handholding on interview preparation process till the time the participant is placed. Guidance is also provided on Linkedin profile building and tricks of the trade to improve the marketability of the resume. – Clininfotech Management