Houser Clinical Research Writing and Consulting

thouser@housercrwc.com

Services Offered by
Houser CRWC

Regulatory and Medical Writing

Clinical Study Reports
Protocols
Investigator Brochures
Safety Narratives
Annual Reports
Informed Consent Forms
Briefing Documents
CRF Completion Guidelines and Study Reference/Procedures Manuals
Submission documents, such as Clinical Overviews, General Investigational Plans, Clinical Summaries
Abstracts and poster compilation

Editing/QA

Slide Presentations

For example:

Safety overview for a compound
Protocol overview for investigator meeting

Other Clinical Scientist Duties

For example:

Study management and monitoring
Database review
Preparing parts of a package to present to management for new indications (study design, comparator compounds)

Document Security
Documents backed up daily:
1. External hard drive and
2. On-line back-up.
Digital ID for secure email via VeriSign
To locate and retrieve digital ID: https://digitalid.verisign.com/services/client/index.html

thouser@housercrwc.com