Title: Drug Safety Pharmacovigilance
1 Pharmacovigilance by Dr. Notghi Contract
Research
2Our Medical Drug Safety Services
- Call Centre
- Drug Safety Data Entry
- Literature Surveillance
- Analysis and Reporting
- Medical writing
- IT Services
3AE/SAE Data Collection Processing
Dr. Notghi CRO Drug Safety Unit
Safety DB
AEs/SAEs entered to DB
Literature
Call Centre
4Call Centre Services
Data Collection
Registration Data Entry
SAE transfer data to Safety Database System
5Web Portal
- Secure web-based portal for data collection
- Product Complaints
- Medical/Technical Inquires
- Adverse Events
6Product and Clinical Trial Safety Monitoring
- AE/SAE Reports (per fax, email, mail)
- Data Entry by trial specific trained personnel
- Quality Check
- Monitor/Investigator contact
- Analysis and Reporting
7Literature Surveillance Process
- Product specific literature database search
- Librarian services
- Data Entry
- Quality Check
- Analysis and Reporting
8Safety Data Retrieval / Data Mining
Dr. Notghi CRO Drug Safety Unit
Safety Data Retrieval and Data Mining
Analysis and Reporting
Client
9IT Services for Medical Drug Safety
- Validation of e.g. ARGUS 3
- Database Maintenance
- Literature database set-up
- Programming, etc.
10Quality Assurance
- Compliance with regulatory requirements
- Client internal quality assessments
- Training
- QC Checks
- Ensuring consistency and validity, coding
accuracy, clinical assessment
11Client Specific Compliance
- Corporate Standard Operating Procedures
- Client SOPs and Working Procedure
- Client Specific Templates
- Client Specific Trial Management Systems and DM
Systems
12Training
- Providing hands-on training for ARGUS
- Concepts and pharmacovigilance procedures
- MedDRA and GCP/ICH training
13Contact
Dr. Notghi Contract Research Zimmerstrasse 55 D-
10117 Berlin-Mitte Germany Tel. 49-30-46064
780 Fax 49-30-46064 733 Email
contact_at_notghi.com Homepage www.notghi.com