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Drug safety
Comprehensive Case Management
Qualified Person (QPPV) support services
Risk Management Services
Medical Review
Literature Search services
Signal Detection
Audit Readiness & Inspection Services
Global aggregate report development
Medical Writing
Narrative Writing
Clinical Trial writing
Review articles
Drug Application
Data Entry and Quality Control
DRUG SAFETY PHYSICIANS
MEDICAL WRITING
Medical Monitoring
Risk Based Monitoring
Regulatory Services
Safety & Medical Monitoring
Clinical Monitoring/ Site Management
Asset Management/ Development
Services
Data and Safety Monitoring Board (DSMB)
Clinical Events Committee (CEC)
Safety Assessment Committees (SAC)
Trial Acceleration
Site Recommendation
Patient Recruitment
Accrual Workshops
Community Research Consortium
Technical Augmentation
Immuno-Oncology
SCP-Technology
ADC Technology
Publishing
Articles
Print Now
NDA/CDA
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Our Services
Clinical Development
Steering Committee Development
Central IRB/ETHIC Committee
Site Management
Clinical Trial Development and Operations
Notifications and Equipment Removal
Accrual and Recruiting Boost
Clinical Data Management and Analysis
Source Data Verification
Drug Safety
Global Medical Monitoring
Clinical Affairs
Diligence
Material checklist
Ownership
Review License Agreements
Freedom to Operate
Ex-US Filings
Patent Term and Exclusivity
Claim Scope
Patent Validity
Evaluation of the Trade secrets
Enforcement challenges/mitigation
Compliance with OIG, CIA and beyond
GAP-IT Services
Brand development with Advertising
Complete Website Transformation
E-Commerce Solutions
GAP- IT US- based Outsourcing
Portal Development
Software Development
Open Source Customization
IT Consulting
Multimedia Services
Graphics and 2D/3D Animation
Search Engine Optimization (SEO)
Website Development
Mergers and Acquisitions
Regulatory and Quality Services
Quality Compliance
Regulatory Compliance
Strategic Consulting
Optimization
Planning
Tool Box
Validation
Technical Augmentation
Immuno-Oncology
SCP-Technology
ADC Technology
Technology Transfer
Featured Services
Patent Term and Exclusivity
Clinical Trial Development and Operations
Medical Affairs
Medical Monitoring
Notifications and Equipment Removal
Quality Compliance
IT Consulting
How We Think
Data Entry and Quality Control
Drug Application
Global aggregate report development
Literature Search services
Regulatory Compliance
Regulatory Services
Review License Agreements
Risk Based Monitoring
Safety & Medical Monitoring
Safety Assessment Committees (SAC)
Trial Acceleration
Site Recommendation
Accrual Workshops
Patient Recruitment
Community Research Consortium
Medical Monitoring
Risk Based Monitoring
Clinical Monitoring/ Site Management
Regulatory Services
Safety & Medical Monitoring
Asset Management/ Development
Publishing
Articles
Books
Print Now
NDA/CDA
Evaluation of the Trade secrets
Work with target to identify key trade secrets
Assess measures in place for protection of key trade secrets
CDAs and non-use agreements
Security measures applied to trade secrets
Is access limited to those who “need to know”
✓ Locked doors/files
✓ Computer passwords
✓ Strong limits on visitors
✓ Limitations on copying
Review written policy for maintaining trade secrets
In-licensed trade secrets
Transferable under license?
Target complying with license?
Scope of license meets needs of acquirer?
Enforcement obligations?
Exclusivity?
Contact us
for more information.