Instructor Led Clinical Trials Training
Clinical Trials Training Provider? - Tell us about your Training!
 online course |
 instructor-led class |
 learn at home |
 group study |
 self-directed study |
 cd-based training |
 DVD video training |
 printed book |
 e-book digital book |
 workshop seminar |
 train the trainer |
 computer-based learning |
 discount pricing |
 online tutorial |
From L'Obel IT-Palaestra
L'Obel Certified PG Diploma in BioInformatics Training in Bangalore
...cular Docking studies a Principles & applications
a Clinical trials & approval
a Example drugs
Associated Software & other online resources
a Chem-X, CombiLibMaker, Dock, Autodock, CombiDock, LIGIN, FTDock, GRAMM, FlexX,
Module IX:
a Project work
Course Duration
------------------------
The duration of the BioInformatics course is 180 Days.
Contact us
more...
...cular Docking studies a Principles & applications
a Clinical trials & approval
a Example drugs
Associated Software & other online resources
a Chem-X, CombiLibMaker, Dock, Autodock, CombiDock, LIGIN, FTDock, GRAMM, FlexX,
Module IX:
a Project work
Course Duration
------------------------
The duration of the BioInformatics course is 180 Days.
Contact us
more...
From IBC Asia (S) Pte Ltd
Auditing Clinical Trials for GCP Compliance 5-6 December 2011 Shanghai
... Quality Assurance Professionals who audit the quality of clinical trials, Clinical Research Associates (CRAs) and Managers, Project Leaders, and Medical Monitors who want to enhance their effectiveness, Regulatory Affairs Professionals responsible for GCP regulatory compliance, Investigators, Study Coordinators and Trial Center Managers who want to learn how to prepare for FDA and sponsor
more...
From Centre for Clinincal Research and Training
Fast Track Certificate Course in Clinical Research - One Month Residential Training
For fresh/ working MBBS, BAMS, BHMS, B. Pharm/ M. Pharm., B. Sc/ M. Sc
Conducted by Centre for Clinical Research and Training (CCRT, Mumbai)
Course Duration: 1 Month - 20 May to 19 June, 2011 (Residential in Navi Mumbai)
Course Level: One Month Residential course, 100% Industry Working Faculty, The course makes you a thorough professional ready for the industry,
Course Content:
New drug
more...
Workshop on Pharmacovigilance & documentation in Clinical trails
For Working Pharma executive, Practicing Doctors & Medical professionals, Fresh Graduates
2 days Workshop for Better Understanding
Course Content:
Day 1 - Pharmacovigilance
Overview of Pharmacovigilance
Adverse drug reaction, concept of safety,
Guidelines & Regulatory aspect of PV
Challanges in Pharmacovigilance
Day 2 a Documentation in CT
Investigators Brochure
Protocol & its
more...
From GlobalCompliancePanel
GMP and Regulatory Expectations for Early IND Products - US Seminar 2012 at San Diego
Overview: Any pharmaceutical worker who must deal with products both in early and latter phases of development should attend this course in order to be aware of the regulatory requirements that will affect operations dealing with these products.
Any pharmaceutical worker who must deal with products both in early and latter phases of development should attend this course in order to be aware of
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From Centre for Clinincal Research and Training
Certificate course in Clinical Research Training at your Convenience correspondence with personal assistance
Certificate Course in Clinical Research Training, Course at your Convenience
( correspondence with personal assistance)
Student doing correspondence can attend a Two 2-day workshopsa ™ in any of our centre.
Conducted by CCRT, Mumbai at New Panvel, Navi Mumbai.
Course Duration: 4 to 6 Months (Weekend Batches)
Course Content:
* New Drug Development Process
* Phases Of Clinical
more...
Certificate Course in Clinical Research Training, Course at your Convenience
( correspondence with personal assistance)
Student doing correspondence can attend a Two 2-day workshopsa ™ in any of our centre.
Conducted by CCRT, Mumbai at New Panvel, Navi Mumbai.
Course Duration: 4 to 6 Months (Weekend Batches)
Course Content:
* New Drug Development Process
* Phases Of Clinical
more...
From Gratisol Labs Llc
Pharmacovigilance Training
...a Clinical Development process
a Different phases of clinical Trials
a Adverse events and its types
a Drug Safety in clinical trials and post marketed drugs
a Different sources of Adverse events reporting
a Different types of AE reporting Forms
a Expedited reporting and its timelines
a Different departments working on Pharmacovigilance
a Roles and responsibilities of
more...
From BioMed Informatics India
BIOINFORMATICS THE FUTURE
Job Oriented Training with Project Experience Certification and Placement Assistance
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Clinical Research Clinical Data Management -CDM Medwin Hospitals Hyderabad
...TIES:
According to Mc Kinsey Report, more than 50, 000 Clinical Trials professionals are needed shortly in successful completion of USFDA/ DCGI Investigational New Drug Applications (INDs).
The report by Ernst & Young states that globalization of Clinical Trials to newer options for the Indian clinical research industry. Excellent Opportunities are available in Abroad / India in this
more...
...TIES:
According to Mc Kinsey Report, more than 50, 000 Clinical Trials professionals are needed shortly in successful completion of USFDA/ DCGI Investigational New Drug Applications (INDs).
The report by Ernst & Young states that globalization of Clinical Trials to newer options for the Indian clinical research industry. Excellent Opportunities are available in Abroad / India in this
more...
Final Semester Projects and Summer Trainings Bioinformatics And Drug Designing Medwin Hospitals
Medwin Hospitals, a Multi Speciality Hospital with excellence in modern health care, having state of the art Infrastructure facilities, Ventures BioMed Informatics in the field of Chemi / Bioinformatics by keeping in view of the tremendous applications in improving the quality of the health care. We are the pioneers in research areas of Bioinformatics & Cheminformatics and had been extensively
more...
SAS Clinical Research Clinical Data Management CDM Bioinformatics Drug Design Training with Live Project Medwin Hospitals
BioMed Informatics Medwin Hospitals a Multi Speciality Hospital with excellence in modern health care, having state of the art Infrastructure facilities is offering the Trainings & Projects in our Ongoing Research areas, since the year of 2000.
a Clinical Research & Clinical Data Management with Project
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)
a SAS, Biostatistics &
more...
