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Inside Cliniminds


Our Pharmacovigilance Training
Partner
Cliniminds USA
Call : +91 9810068241 or usa@cliniminds.com
United States is the global destination for clinical trials, and the largest pharmaceutical market in the world. There are several career opportunities in clinical trials, pharmacovigilance, clinical data management, medical writing, drug regulatory affairs and several other areas of health sciences.
There are opportunities for life sciences professional, including medical doctors and other medical sciences professionals, pharmacy, nursing, biotechnology, microbiology, biochemistry and life sciences graduates and post graduates. Professional program would equip you with the right skill set, and would help you in targeting the appropriate job opportunity.
Established in 2004, Cliniminds offers range of online programs for the students from North America. These programs are in the field of clinical trials, pharmacovigilance / drug safety, clinical data management, SAS, medical writing, drug regulatory affairs, and several other programs. Programs are accredited by Accreditation Council for Clinical Research Education (ACCRE), US.
These programs are affordable, job oriented, flexible, and students could complete the program at their own pace. Upon enrolment, students would receive online access to the learning material and printed books.
Online Classes: If any student would like to opt for online interactive sessions with the faculty, there are separate charges for those sessions.
Exams:All exams are online in multiple choice questions format.
Certification: Original certificate would be dispatched at your registered address. Online certificate would be available as soon as you complete the program.
Profile of Cliniminds US Centre Program Consultant:
  • Experienced Drug Safety professional with over 12 years of experienceat various levels in small to mid-sized Bio-pharmaceutical companies in the USA
  • Responsible for all Pharmacovigilance activities for marketed and investigational drug products
  • Authored and ensured that individual SUSAR reports and aggregate safety reports (PSURs, DSURs) for FDA and EU regulatory authorities were completed and submitted in accordance with regulatory requirements
  • Worked on a CCSIs of marketed products
  • Reviewed Protocols and Investigator Brochures
  • Chaired the Medical Safety Review committee which is established to monitor the safety of the products in clinical development and/or in the Market. Activities include but are not limited to identification of potential product specific safety signals/trends, AE case series review, review of scientific literature, review and updates to product labels
  • Created and maintained Pharmacovigilance and Safety Data Exchange Agreements; served as company/partner liaison; ensured corporate and partner compliance with internal and global regulatory requirements
  • Participated in the development of and provided oversight for the REMS program for a CNS product
  • Participated in successful FDA audits for Pharmacovigilance
  • Developed SOPs and Work Practice guidelines for Drug Safety department throughout the life cycle of the product (pre and post marketing) and centralized Drug Safety functions at various companies
  • Responsible for handling safety related activities including receipt, triage, processing, reporting and dissemination of Adverse Events and Serious Adverse Events (SAE) from spontaneous sources and SAE’s from company sponsored clinical trials
  • Supported case processing activities by performing medical review of the cases and assessing the expedited reporting
  • Managed the activities of Drug Safety vendor for AE case processing
For more information on the programs, please refer program section or contact us +91 9810068241 or email at usa@cliniminds.com
+91-9910068241
+91-9560102589
+91-9810068241
Google Reviews

Anushree Jaiswal
Stars I had completed M.pharm in cology in 2013 and after that i did 3 years Job then after the inspiration by Mr. Kamal the director of Cliniminds he told me about the impact of Vigilance and clinical research in current industry and influenced me to join the Course of Pharmacovigilance and clinical research. ...more

Zeba ahmed
Stars I am a BDS professional.I joined cliniminds to accomplish advanced post graduate diploma in pharmacovigilance with software training.Quality teaching is what defines this course the best.From the management itself to the study material to the online classes-everything was taken care of ...more

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Dr. Subodh Bhardwaj
MD (Pharmacology) - Director of Health Sciences Education & Training
A innovative Medical Doctor with post - graduation in Pharmacology and more than 30+ years of experience in
Clinical Medicine, Clinical Research, Pharmacovigilance and Drug Regulatory Affairs.Read More...
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