trialmedlife.com
:: Welcome to TrialMed Life Sciences ::
http://www.trialmedlife.com/index.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. We also extend our services to VCs and incubators to evaluate new medical technology and suggest the best clinical and regulatory option. Our method of operation is to mak...
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/medical_affairs.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. Case Report Forms CRFs Design. Interim and Final Clinical Study Reports (CSRs). Integrated Summaries of Efficacy and Safety. Common Technical Documents (CTDs).
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/content.php?sid=Mzk
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. We were founded in 2000 and based in Irvine, CA with affiliate international offices in Warren, NJ and India. We enjoy a strong reputation with the clinical community.
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/content.php?sid=MjU
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. Our clients can utilize our services in four strategic steps:. Request an at cost evaluation of your clinical and regulatory needs. Site Qualification and Training.
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/staffing_recruitment_services.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. Staffing and Recruitment Services. Our team is your team. Areas of recruitment discipline:. CRCs-Clinical research coordinators (offsite and in-house). Alliance Partners :...
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/trial_crisis_management.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. Site Qualification and Training. Staffing and Recruitment Services. TrialMed India Clinical Trial Institute. Alliance Partners : Blue Square Consulting.
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/downloads.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. Site Qualification and Training. Staffing and Recruitment Services. TrialMed India Clinical Trial Institute. Alliance Partners : Blue Square Consulting.
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/usefullinks.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. Food and Drug Administration (FDA). Association of Clinical Research Professionals (ACRP). American Medical Association (AMA). The Biotechnology Industry Organization.
trialmedlife.com
Welcome to Trial Med Sciences
http://www.trialmedlife.com/trialmed_india_clinical_trial_inst.php
Clinical Site Qualification and Initiation. Patient Rectuitment and Retention. Medical Monitoring and Adverse Event Reporting. Regulatory Affairs- US FDA Interaction. Clinical trial design / protocol / CRF. Clinical Site Services - ICH/GCP Training. Medical Affairs- Technology assessment/medical writing. Data Management and Statistics. TrialMed India Clinical Trial Institute. Our training is customized to assist research professional to work with pharmaceutical, medical device and biologic clinical trials.