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Quality Assurance Services
GVK Biosciences (GVK BIO) Clinical Research division
has an independent Quality Assurance (QA) unit which

The Quality Assurance department coordinates
training of clinical research staff to ensure continuous

conducts audits of services of all business lines within
the division on a routine basis to ensure delivery of

improvement and updating of clinical regulations.

quality services. The Clinical Research QA staff report
to the Director-QA, GVK BIO who in turn reports to the

Team Expertise

CEO of GVK BIO. In addition to providing routine
internal quality assurance support, GVK BIO's QA team

The QA team has a combined experience of over 20
years. Director-QA, has vast experience in the

also provides auditing services to its clients.

development of Quality Systems and handling GCP /
GLP audits successfully by various regulatory agencies

Following are the types of audits we conduct:

like USFDA, WHO (World Health Organization),
AFSSAPS (France), Ministry of Health (Turkey), ANVISA

• Study specific site audits to ascertain compliance
to protocol, GCP and regulatory requirements
• Study specific Clinical Operations audits at start
up, ongoing and close-out phases of the study
• Clinical database audits are conducted before the
database is moved to production, interim
database audit and database audit before
database lock
• Biostatistics audits covering quality review of
tables, data listings, and study reports

(Brazil) and GCP / GLP audits of multinational
companies.

About GVK BIO
GVK Biosciences (GVK BIO) is Asia’s leading Discovery
Research and Development organization. GVK BIO
provides a broad spectrum of services, stand-alone
and integrated, across the R&D value chain.
Services
• Chemistry Services

• Project specific medical affairs audits to ensure
compliance to protocol, regulatory requirements,
client agreements and GCP

• Process R&D and Custom Synthesis

• Process oriented audits across different
functions and business lines within Clinical
Research

• Clinical Research

• Contract audits on behalf of sponsor/ health
authorities at the sites

• Biology
• Informatics
• Clinical Pharmacology
Contact: bdcrd@gvkbio.com
Visit: www.gvkbio.com

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Quality Assurance Services

  • 1. sd Quality Assurance Services GVK Biosciences (GVK BIO) Clinical Research division has an independent Quality Assurance (QA) unit which The Quality Assurance department coordinates training of clinical research staff to ensure continuous conducts audits of services of all business lines within the division on a routine basis to ensure delivery of improvement and updating of clinical regulations. quality services. The Clinical Research QA staff report to the Director-QA, GVK BIO who in turn reports to the Team Expertise CEO of GVK BIO. In addition to providing routine internal quality assurance support, GVK BIO's QA team The QA team has a combined experience of over 20 years. Director-QA, has vast experience in the also provides auditing services to its clients. development of Quality Systems and handling GCP / GLP audits successfully by various regulatory agencies Following are the types of audits we conduct: like USFDA, WHO (World Health Organization), AFSSAPS (France), Ministry of Health (Turkey), ANVISA • Study specific site audits to ascertain compliance to protocol, GCP and regulatory requirements • Study specific Clinical Operations audits at start up, ongoing and close-out phases of the study • Clinical database audits are conducted before the database is moved to production, interim database audit and database audit before database lock • Biostatistics audits covering quality review of tables, data listings, and study reports (Brazil) and GCP / GLP audits of multinational companies. About GVK BIO GVK Biosciences (GVK BIO) is Asia’s leading Discovery Research and Development organization. GVK BIO provides a broad spectrum of services, stand-alone and integrated, across the R&D value chain. Services • Chemistry Services • Project specific medical affairs audits to ensure compliance to protocol, regulatory requirements, client agreements and GCP • Process R&D and Custom Synthesis • Process oriented audits across different functions and business lines within Clinical Research • Clinical Research • Contract audits on behalf of sponsor/ health authorities at the sites • Biology • Informatics • Clinical Pharmacology Contact: bdcrd@gvkbio.com Visit: www.gvkbio.com