QVIS - Quality & Pharmacovigilance Specialists

Quality Management Service

· Services provided by certified auditors
· Risk-based Quality Assurance Services
· Standard Operating Procedure Development
· GCP, GCLP, and GVP audits
· Management of non-compliance and violations

SOP Development

We provide comprehensive SOP development services
according to sponsor-specific requirements, ICH-GCP,
and European and U.S. clinical trial regulations.
SOP development areas are listed below and can be prepared in Korean or English.

We provide comprehensive SOP development services according to sponsor-specific requirements, ICH-GCP, and European and U.S. clinical trial regulations.
SOP development areas are listed below and can be prepared in Korean or English.

· Clinical trial-related work including clinical operations
· Quality assurance for clinical trials
· Pharmacovigilance-related work

Global Compliance Consultant

QVIS provides professional, internationally aligned consulting services
from the planning stage of clinical trials so that studies can be conducted with quality
within planned costs and timelines.

QVIS provides professional, internationally aligned consulting services from the planning stage of clinical trials so that studies can be conducted with quality within planned costs and timelines.

· Project Planning
· CRO Selection
· Protocol Quality by Design
· Core Document review

ABOUT US

· QVIS was established in August 2014
as Korea's first company specializing
in clinical trial quality assurance.
· QVIS was established in August 2014 as Korea's first company specializing in clinical trial quality assurance.
· QVIS provides quality assurance services
in GCP, GLP(GCLP), and GVP, and consists of
auditors certified by SQA or RQA.
· QVIS provides quality assurance services in GCP, GLP(GCLP), and GVP, and consists of auditors certified by SQA or RQA.
· QVIS provides pharmacovigilance services
from new drug development through
post-marketing stages with US certified safety officers.
· QVIS provides pharmacovigilance services from new drug development through post-marketing stages with US certified safety officers.
· QVIS has experience across diverse therapeutic areas,
investigational sites, pharmaceutical companies,
and CROs in Korea, Asia, and the United States.
· QVIS has experience across diverse therapeutic areas, investigational sites, pharmaceutical companies, and CROs in Korea, Asia, and the United States.

CORE VALUES

Independence
QVIS pursues independence
in quality assurance and pharmacovigilance
through independent organizational operations.
QVIS pursues independence in quality assurance and pharmacovigilance through independent organizational operations.
Reliability
QVIS pursues reliable services
by providing professional work based on
responsibility and ethics.
QVIS pursues reliable services by providing professional work based on responsibility and ethics.
Professionalism
QVIS pursues professionalism
through continuous training and experience sharing
by experts in drug development and pharmacovigilance.
QVIS pursues professionalism through continuous training and experience sharing by experts in drug development and pharmacovigilance.

SCOPE OF SERVICE

Please send inquiries using the form below. We will respond as soon as possible.

LOCATION

ADDRESS.

TEL.
E-mail.

#611, #612, 25, Yeonmujang 5ga-gil,
Seongdong-gu, Seoul 04782, Korea
+82-2-6925-0320
Business Development

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