Pharma Consulting
Arround 10 years experience in pharmaceutical industry on a local and global level with hands-on approach.
About Me
Flexible, open-minded and proactive to support any need you may have in pharmaceutical project management.
Pharmacovigilance
All aspects of case processing. Click below to get more information.
Clinical Trials
Clinical Trial Coordinator in alignment to ICH-GCP standard.
Contact
Flexible, open-minded and proactive to support any need you may have.
Pharmacovigilance
All aspects of case processing such as:
Data Management
Performing Data Management of Clinical Safety & Pharmacovigilance information of individual case safety reports (ICSR)
Data entry
Data entry, coding according to MedDRA terminology, writing of narratives from adverse events into global safety data base
Data reconciliation
Data collection
Data collection and review of incoming information on ICSRs
Case distribution
Case distribution to Regulatory Authorities, Ethics Committees, Investigators, license partners and company’s affiliates via electronic report
Case tracking
Clinical Trials
Clinical Trial Coordinator in alignment to ICH-GCP standard
Why Choose Us
Various indications and phases
Site evaluation, initiation, monitoring and close-out visits
TMF / e-TMF
Flexible, open-minded and proactive to support any need you may have in pharmaceutical project management.
Clients
Yrs in Business
HM Pharma Consulting
Arround 10 years experience in pharmaceutical industry on a local and global level with hands-on approach.
Contact us
Call Us
(+49) 172 8945 800
Email Us
info@hm-pharma-consulting.de
Our Location
Hauptstr. 39
89343 Jettingen-Scheppach
Germany