Instructor Led Gcp Training
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 online course |
 instructor-led class |
 learn at home |
 group study |
 self-directed study |
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 DVD video training |
 printed book |
 e-book digital book |
 workshop seminar |
 train the trainer |
 computer-based learning |
 discount pricing |
 online tutorial |
From Clinical Research Training Centre
Job Placement Assistance Program in Clinical Research
On-line and In-class Clinical Research Job Placement Assistance Program for health & life science professionals (3 courses in 1)
1. Clinical trial conduct regulations in Canada, USA and EMEA
2. Job search methods adapted to the clinical research
3. How to reach the 90% hidden jobs - Networking 2. 0
Optional Virtual Internship program to get "hands-on" monitoring experience. The program
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On-line and In-class Clinical Research Job Placement Assistance Program for health & life science professionals (3 courses in 1)
1. Clinical trial conduct regulations in Canada, USA and EMEA
2. Job search methods adapted to the clinical research
3. How to reach the 90% hidden jobs - Networking 2. 0
Optional Virtual Internship program to get "hands-on" monitoring experience. The program
more...
Assistance Placement en Recherche Clinique
Programme d'assistance au placement en recherche clinique pour professionnels des sciences de la sant et sciences de la vie qui veulent travaille dans l'administration des essais cliniques donn en ligne et en classe (3 cours en 1).
1. R glementation canadienne, am ricaine et europ enne sur la conduite et le monitorage des essais cliniques
2. M thodes de recherche d'emploi, adapt
more...
Programme d'assistance au placement en recherche clinique pour professionnels des sciences de la sant et sciences de la vie qui veulent travaille dans l'administration des essais cliniques donn en ligne et en classe (3 cours en 1).
1. R glementation canadienne, am ricaine et europ enne sur la conduite et le monitorage des essais cliniques
2. M thodes de recherche d'emploi, adapt
more...
From IBC Asia (S) Pte Ltd
Auditing Clinical Trials for GCP Compliance 5-6 December 2011 Shanghai
...iveness, 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 audits and to improve the quality of their research activities. Participants will learn practical, immediately usable techniques which top-notch Good Clinical Practice (GCP) auditors and FDA
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From Centre for Clinincal Research and Training
Certificate Course in Clinical Research
Clinical Research certificate course 6 months Part time weekend
CDM, Medical writing, Pharmacovigilance, Regulatory Affairs etc
Starting at
1. New Panvel, Navi Mumbai
From 7th May 2011 Time 10am to 2pm
2. Prin K. M. Kundanani College, Cuffe Parade, Mumbai
From July 2011 Time 2pm to 6pm
3. Nasik, Maharashtra
From July 2011 Time 10am to 2pm
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Clinical Research certificate course 6 months Part time weekend
CDM, Medical writing, Pharmacovigilance, Regulatory Affairs etc
Starting at
1. New Panvel, Navi Mumbai
From 7th May 2011 Time 10am to 2pm
2. Prin K. M. Kundanani College, Cuffe Parade, Mumbai
From July 2011 Time 2pm to 6pm
3. Nasik, Maharashtra
From July 2011 Time 10am to 2pm
more...
From BioMed Informatics India
Trainings & Projects SAS Clinical Research Clinical Data Management CDM Bioinformatics and Drug Design Medwin Hospitals Hyder
...rch & Clinical Data Management with Project
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)
Bioinformatics/ Cheminformatics with Project
(Molecular Modeling & Computer Aided Drug Design)
SAS, Biostatistics & Project in Clinical Research
Our Students are employed in Satyam Computers, Apollo Hospitals,
Quintiles, Novartis, Reliance Life Sciences, Glenmark
more...
...rch & Clinical Data Management with Project
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)
Bioinformatics/ Cheminformatics with Project
(Molecular Modeling & Computer Aided Drug Design)
SAS, Biostatistics & Project in Clinical Research
Our Students are employed in Satyam Computers, Apollo Hospitals,
Quintiles, Novartis, Reliance Life Sciences, Glenmark
more...
Clinical Research Clinical Data Management -CDM Medwin Hospitals Hyderabad
...Clinical Research & Clinical Data Management -CDM
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)
Medwin Hospitals, a Multi Speciality Hospital with excellence in modern health care ventures BioMed Informatics in the field of Clinical Research by keeping in view of the tremendous applications in improving the quality of the health care.
Clinical Research comprises of ICH-GCP
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...Clinical Research & Clinical Data Management -CDM
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)
Medwin Hospitals, a Multi Speciality Hospital with excellence in modern health care ventures BioMed Informatics in the field of Clinical Research by keeping in view of the tremendous applications in improving the quality of the health care.
Clinical Research comprises of ICH-GCP
more...
SAS Clinical Research Clinical Data Management CDM Bioinformatics Drug Design Training with Live Project Medwin Hospitals
... Research & Clinical Data Management with Project
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)
a SAS, Biostatistics & Project in Clinical Research
a Bioinformatics/ Cheminformatics with Project
(Molecular Modeling & Computer Aided Drug Design)
Our Students are employed in Satyam Computers, ICMR, Apollo Hospitals, Quintiles, Novartis, Reliance Life Sciences, Glenmark
more...
From Clinical Research Solutions
Good Clinical Practice GCP Workshop
Good Clinical Practice Workshop
This workshop covers the ICH-GCP regulations, with a particular focus on investigator responsibilities. It covers the following topics
-A history of the main events and documents leading to ICH GCP
-ICH-GCP guidelines with focus on investigator responsibilities, informed consent, source documents and adverse event reporting
-Hands-on exercise dealing with
more...
Good Clinical Practice Workshop
This workshop covers the ICH-GCP regulations, with a particular focus on investigator responsibilities. It covers the following topics
-A history of the main events and documents leading to ICH GCP
-ICH-GCP guidelines with focus on investigator responsibilities, informed consent, source documents and adverse event reporting
-Hands-on exercise dealing with
more...
