SOLUTIONS
Clinical Development
Full Service
Early Development
Phase II - IV
Medical Devices
Functional Service Provider
Concept Development & Study Design
Site Selection & Activation
Clinical Study Management
Clinical Site Monitoring
Data Management
Statistical Analysis
Regulatory Affairs
Pharmacovigilance
Clinical Quality Compliance & Auditing
IMP Management
Medical Writing
Medical Translation Services
Therapeutic Expertise
iCOS
Real World Data
Registries & Observational Studies
Patient Reported Outcomes
Pharmacoeconomic Studies
Post Authorisation Safety Studies
Post Authorisation Efficacy Studies
Commercialization
Contract Detailing Services
Medical & Scientific Affairs
Medical Writing
Market Research & Analysis
Market Access
Vigilance
Regulatory Affairs
Training & Learning
OUR COMPANY
Who We Are
Leadership
Compliance & Ethics
Quality Policy
Business Continuity Policy
Information Security Policy
Data Protection Policy
Anti-Corruption and Anti-Bribery Policy
Whistleblowing Policy
Medical Devices Policy
Name Origination
CONTACT US
CAREERS
QA & IT Associate - Job Code: QA-2022010
Clinical Operation Manager - Job Code: CL-2022009
Regulatory Affairs Associate - Job Code: RA-2021009
Regulatory Affairs Manager - Job Code: RA-2019005
Detailer - Job Code: DE-2018005
Detailer - Job Code: DE-2018006
Clinical Research Associates - Job Code: CL-2018008
Detailer - Job Code: DE-2018009-THE
Detailer - Job Code: DE-2018009-LAR
Detailer - Job Code: DE-2018009-ATH
COMMERCIALIZATION
Dermatology
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Our Solutions
Clinical Development
Full Service
Early Development
Phase II - IV
Medical Devices
Functional Service Provider
Concept Development & Study Design
Site Selection & Activation
Clinical Study Management
Clinical Site Monitoring
Data Management
Statistical Analysis
Regulatory Affairs
Pharmacovigilance
Clinical Quality Compliance & Auditing
IMP Management
Medical Writing
Medical Translation Services
Therapeutic Expertise
iCOS
Real World Data
Registries & Observational Studies
Patient Reported Outcomes
Pharmacoeconomic Studies
Post Authorisation Safety Studies
Post Authorisation Efficacy Studies
Commercialization
Contract Detailing Services
Medical & Scientific Affairs
Medical Writing
Market Research & Analysis
Market Access
Vigilance
Regulatory Affairs
Training & Learning
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CLINICAL DEVELOPMENT
The fast delivery of quality results is the “code of ethics” in our work and our
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REAL WORLD DATA
This is the time that some of the most important questions start looking for an answer.
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VIGILANCE
Patients' safety and well-being are paramount for your product’s safety profile and overall effectiveness thus encompasses
…
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