Cliniminds India

Cliniminds India An Academy for Clinical Research and Healthcare Training & Management. https://cliniminds.com/

Cliniminds to Offer High Quality Professional Training Programs in Clinical Research

Cliniminds is an innovative clinical research training institute providing a wide range of clinical trials training solutions to the students, pharmaceutical companies, CROs and healthcare companies globally. Cliniminds was established in year 2004, by a group of professionals from Clinical Research, Pharmaceutical industry and Healthcare industry with rich and varied experience at senior management levels. Company was set up with the objective to offer education and training solutions in the field of clinical research, pharmaceuticals and healthcare. Cliniminds today is one of the best clinical research training institutes. Cliniminds clinical research programs enjoy very high level of acceptance from leading global pharmaceutical and clinical research companies. Cliniminds Online Programs are popular amongst the students from India, USA, Mexico, U.K., Canada, Europe, Africa, Asia and Middle East. Cliniminds today is the leader in the clinical research education and training domain. Today Cliniminds is being rated amongst the best quality clinical research institutes globally. Good Clinical Practice (GCP) guidelines and regulations of respective countries govern conduct of clinical trials, and a thorough knowledge of procedures at every stage of the clinical trial process is essential. Cliniminds can help you achieve the level of expertise required through our high quality, user-friendly and cost-effective training programs - whether you need to train for a career in clinical trials, or update your knowledge with current information.

Advanced Post Graduate Diploma in Medical Devices Clinical & Regulatory AffairsBatch Commencement – 1st March 202611 Mon...
02/02/2026

Advanced Post Graduate Diploma in Medical Devices Clinical & Regulatory Affairs

Batch Commencement – 1st March 2026

11 Months | Live eLearning (Weekends)

Contact Us Now: +91-9310485979

Mail Us On: info@cliniminds.com

Visit Us On: https://cliniminds.com/medical-devices-course

ClinicalResearch ClinicalAffairs MedicalDeviceRegulatory RAProfessionals RegulatoryExpertise MedicalDeviceCareers DrugsToDevices QMS ISO13485 ISO9001 IVD SaMD CombinationProducts HealthcareCareers LifeSciences PostGraduateDiploma WeekendLearning LiveELearning CareerUpgrade RegulatoryJobs HealthcareTraining MedicalTechnology RegulatoryEducation ClinicalTraining SkillDevelopment

https://youtu.be/83XhvdwTAPEDrug Master File & Regulatory Filling System - Cliniminds Drug Regulatory AffairsA Drug Mast...
02/02/2026

https://youtu.be/83XhvdwTAPE
Drug Master File & Regulatory Filling System - Cliniminds Drug Regulatory Affairs
A Drug Master File (DMF) is a confidential submission made to the FDA that provides detailed information about the Chemistry, Manufacturing and Controls (CMC) related to a drug or one of its components.

regulatory

A Drug Master File (DMF) is a confidential submission made to the FDA that provides detailed information about the Chemistry, Manufacturing and Controls (CMC...

Mastering Medical Device Clinical & Regulatory AffairsCliniminds Advanced PG Diploma in Medical Device Clinical & Regula...
02/02/2026

Mastering Medical Device Clinical & Regulatory Affairs

Cliniminds Advanced PG Diploma in Medical Device Clinical & Regulatory Affairs is designed to bridge the global skill gap for life sciences professionals. This 11-month weekend learning program offers flexible live sessions, hands-on practical training, and industry-led faculty guidance. The course provides comprehensive exposure to global regulatory frameworks including US FDA, EU MDR, and CDSCO, with specialized focus on SaMD, IVDs, and combination products. Learners gain dual global accreditations, 24/7 LMS access, capstone projects, and mentorship for real-world regulatory and clinical excellence.

Drug Master File & Regulatory Filling System - Cliniminds Drug Regulatory AffairsA Drug Master File (DMF) is a confident...
31/01/2026

Drug Master File & Regulatory Filling System - Cliniminds Drug Regulatory Affairs

A Drug Master File (DMF) is a confidential submission made to the FDA that provides detailed information about the Chemistry, Manufacturing and Controls (CMC) related to a drug or one of its components.

https://youtu.be/83XhvdwTAPE

regulatory

A Drug Master File (DMF) is a confidential submission made to the FDA that provides detailed information about the Chemistry, Manufacturing and Controls (CMC...

eTMF Software - Cliniminds Clinical ResearcheTMF (Electronic Trial Master File) software in clinical research is a digit...
31/01/2026

eTMF Software - Cliniminds Clinical Research

eTMF (Electronic Trial Master File) software in clinical research is a digital system for securely managing, storing, and tracking all essential documents for a clinical trial, replacing paper files to ensure regulatory compliance, improve efficiency, and provide real-time visibility for sponsors, CROs, and sites.

https://youtu.be/ATiPBcXqPzw

eTMF (Electronic Trial Master File) software in clinical research is a digital system for securely managing, storing, and tracking all essential documents fo...

Advanced Post Graduate Diploma in Medical Devices Clinical & Regulatory AffairsBatch Commencement – 1st March 202611 Mon...
31/01/2026

Advanced Post Graduate Diploma in Medical Devices Clinical & Regulatory Affairs

Batch Commencement – 1st March 2026

11 Months | Live eLearning (Weekends)

Contact Us Now: +91-9310485979

Mail Us On: info@cliniminds.com

Visit Us On: https://cliniminds.com/medical-devices-course

RAProfessionals DrugsToDevices RegulatoryExpertise MedicalDeviceCareers ClinicalAffairs QMS IVD SaMD CombinationProducts HealthcareCareers LifeSciences

Post Graduate Diploma with Job Placements Drug Regulatory Affairs, IPR & PatentsContact: +91-95601 02589Registration: ht...
31/01/2026

Post Graduate Diploma with Job Placements Drug Regulatory Affairs, IPR & Patents

Contact: +91-95601 02589

Registration: https://cliniminds.com/dra

PostGraduateDiploma JobPlacements AssuredInterviews drug ipr patents

Post Graduate Diploma with Job Placements Drug Regulatory Affairs, IPR & PatentsContact: +91-95601 02589Registration: ht...
31/01/2026

Post Graduate Diploma with Job Placements Drug Regulatory Affairs, IPR & Patents

Contact: +91-95601 02589

Registration: https://cliniminds.com/dra

PostGraduateDiploma

Address

B8 Noida One, Sector 62 Office No. 602, 6th Floor, Tower B
Noida
201309

Opening Hours

Monday 9:30am - 6pm
Tuesday 9:30am - 6pm
Wednesday 9:30am - 6pm
Thursday 9:30am - 6pm
Friday 9:30am - 6pm
Saturday 9:30am - 5pm
Sunday 9:30am - 2pm

Telephone

+919810068241

Website

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